{"product_id":"5-bromopyridine-2-carbonitrile-cas-97483-77-7","title":"5-Bromopyridine-2-carbonitrile | CAS 97483-77-7 | ≥98%","description":"\u003cdiv style=\"margin-bottom: 28px;\"\u003e\n\u003cdiv style=\"background: #002147; padding: 10px 20px; margin-bottom: 0;\"\u003e\n\u003ch3 style=\"margin: 0; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; font-size: 0.70em; font-weight: bold; letter-spacing: 0.12em; text-transform: uppercase; color: #fff;\"\u003eTechnical Specifications\u003c\/h3\u003e\n\u003c\/div\u003e\n\u003ctable style=\"width: 100%; border-collapse: collapse; font-size: 0.95em; border: 1px solid #e4e8f0; border-top: none; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif;\"\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eCAS Number\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003e97483-77-7\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eEC \/ EINECS Number\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003e628-634-9\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eMDL Number\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003eMFCD00234144\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eSMILES\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0; word-break: break-all;\"\u003eC1=CC(=NC=C1Br)C#N\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eInChI\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0; word-break: break-all;\"\u003eInChI=1S\/C6H3BrN2\/c7-5-1-2-6(3-8)9-4-5\/h1-2,4H\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eInChIKey\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0; word-break: break-all;\"\u003eDMSHUVBQFSNBBL-UHFFFAOYSA-N\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003ePubChem CID\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003e817154\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eMolecular Formula\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003eC₆H₃BrN₂\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eMolecular Weight\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003e183.01 g\/mol\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eMelting Point\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003e128–132 °C\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eSolubility\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003eSoluble in methanol, acetonitrile, DMF, THF and DMSO.\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003ePurity\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003e≥98%\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003ePhysical Form\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003eWhite to light yellow powder or crystals\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eHS Code\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003e2933.39\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; border-bottom: 1px solid #e4e8f0; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eShelf Life\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333; border-bottom: 1px solid #e4e8f0;\"\u003eRetest period: 36 months from date of manufacture\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"padding: 9px 16px; font-weight: 600; color: #002147; width: 200px; background: #f7f8fb; font-size: 0.95em; vertical-align: top;\"\u003eStorage Conditions\u003c\/td\u003e\n\u003ctd style=\"padding: 9px 16px; color: #333;\"\u003eStore in a cool, dry, well-ventilated place in a tightly sealed container, protected from light.\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"margin-bottom: 28px;\"\u003e\n\u003cdiv style=\"background: #002147; padding: 10px 20px; margin-bottom: 0;\"\u003e\n\u003ch3 style=\"margin: 0; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; font-size: 0.70em; font-weight: bold; letter-spacing: 0.12em; text-transform: uppercase; color: #fff;\"\u003eProduct Description \u0026amp; Scientific Applications\u003c\/h3\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"padding: 16px 20px; border: 1px solid #e4e8f0; border-top: none; font-family: Georgia, 'Times New Roman', serif; font-size: 0.95em; line-height: 1.65; color: #333;\"\u003e\n\u003cdiv\u003e\n\u003cp\u003e\n\u003cstrong\u003e5-Bromopyridine-2-carbonitrile\u003c\/strong\u003e is a pyridine with a bromine atom at C-5 and a nitrile group at C-2.\u003c\/p\u003e\n\u003cp\u003e\n\u003cstrong\u003eSuzuki and Heck coupling.\u003c\/strong\u003e Under Suzuki conditions it couples with substituted phenylboronic acids to give 5-aryl-2-pyridinecarbonitriles. It also gives a dinitrile in a Heck coupling with 2,2′-bifuran-5-carbonitrile.\u003c\/p\u003e\n\u003cdiv style=\"margin:8px 0 18px 0;\"\u003e\n\u003cdiv style=\"display:flex;flex-wrap:wrap;align-items:center;justify-content:flex-start;gap:2px;\"\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"140px\" height=\"100px\" viewbox=\"0 0 140 100\"\u003e\n\u003cpath d=\"M 24,24.2 L 38.4,32.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 25.6,21.3 L 40.1,29.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 22.4,27 L 36.8,35.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 38.4,32.4 L 57.6,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 57.6,43.2 L 57.7,65.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 57.7,65.2 L 76.8,76.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 61,63.3 L 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fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"111\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eB\u003c\/text\u003e\n\u003ctext x=\"120.1\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"72.6\" y=\"38.7\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003cdiv style=\"font-size:20px;padding:0 4px;align-self:center;\"\u003e+\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"100px\" height=\"80px\" viewbox=\"0 0 100 80\"\u003e\n\u003cpath d=\"M 49.3,29.4 L 49.3,39.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 54,46.8 L 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style=\"display:flex;flex-direction:column;align-items:center;justify-content:center;min-width:90px;max-width:150px;padding:0 4px;text-align:center;font-size:12px;line-height:1.3;\"\u003e\n\u003cdiv\u003eSuzuki coupling\u003c\/div\u003e\n\u003cdiv style=\"font-size:30px;line-height:1;\"\u003e⟶\u003c\/div\u003e\n\u003cdiv\u003ePd catalyst, base\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"150px\" height=\"100px\" viewbox=\"0 0 150 100\"\u003e\n\u003cpath d=\"M 29.3,24.2 L 43.7,32.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 30.9,21.3 L 45.4,29.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 27.7,27 L 42.1,35.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 43.7,32.4 L 62.9,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 62.9,43.2 L 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stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003ctext x=\"20.7\" y=\"28.1\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"116.3\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eA\u003c\/text\u003e\n\u003ctext x=\"125.4\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"77.9\" y=\"38.7\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp style=\"font-size:12px;margin:4px 0 0 0;\"\u003e\n\u003cem\u003eGeneral reaction: 5-bromopyridine-2-carbonitrile + aryl boronic acid → 5-aryl-2-pyridinecarbonitrile.\u003c\/em\u003e\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e\n\u003cstrong\u003eAmidines from the nitrile.\u003c\/strong\u003e Azaterphenyl diamidines have been made from it in two steps, starting with coupling to 1,4-phenylenebisboronic acid. In that route, the bis-nitriles were converted to the diamidines with LiN(TMS)\u003csub\u003e2\u003c\/sub\u003e in THF. These diamidines were evaluated for in vitro antiprotozoal activity.\u003c\/p\u003e\n\u003cdiv style=\"margin:8px 0 18px 0;\"\u003e\n\u003cdiv style=\"display:flex;flex-wrap:wrap;align-items:center;justify-content:flex-start;gap:2px;\"\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"150px\" height=\"100px\" viewbox=\"0 0 150 100\"\u003e\n\u003cpath d=\"M 29.3,24.2 L 43.7,32.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 30.9,21.3 L 45.4,29.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 27.7,27 L 42.1,35.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 43.7,32.4 L 62.9,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 62.9,43.2 L 63,65.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 63,65.2 L 82.1,76.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 66.3,63.3 L 82.1,72.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 82.1,76.1 L 101.1,65\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 101.1,65 L 115.5,73.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 101.1,65 L 101,43\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 97.8,63.1 L 97.7,44.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 101,43 L 86.5,34.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 77.2,34.9 L 62.9,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 78.8,37.7 L 66.2,45.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 43,32 L 43.7,32.4 L 44.7,32.9\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 63,64.1 L 63,65.2 L 64,65.8\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 81.2,75.6 L 82.1,76.1 L 83.1,75.6\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 101,44.1 L 101,43 L 100.2,42.6\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003ctext x=\"20.7\" y=\"28.1\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"116.3\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eA\u003c\/text\u003e\n\u003ctext x=\"125.4\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"77.9\" y=\"38.7\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003cdiv style=\"display:flex;flex-direction:column;align-items:center;justify-content:center;min-width:90px;max-width:150px;padding:0 4px;text-align:center;font-size:12px;line-height:1.3;\"\u003e\n\u003cdiv\u003e1. LiN(TMS)\u003csub\u003e2\u003c\/sub\u003e, THF\u003c\/div\u003e\n\u003cdiv style=\"font-size:30px;line-height:1;\"\u003e⟶\u003c\/div\u003e\n\u003cdiv\u003e2. HCl, EtOH\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"160px\" height=\"110px\" viewbox=\"0 0 160 110\"\u003e\n\u003cpath d=\"M 122.6,54.9 L 107.4,63.7\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 120.9,52.1 L 105.8,60.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 107.4,61.8 L 107.4,79.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 107.4,61.8 L 88.3,50.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 88.3,50.8 L 69.3,61.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 69.3,61.8 L 50.2,50.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 69.3,58 L 53.5,48.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 50.2,50.9 L 50.2,28.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 50.2,28.9 L 33.9,19.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 50.2,28.9 L 69.3,17.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 53.5,30.8 L 69.3,21.7\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 69.3,17.8 L 83.6,26.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 88.3,36.1 L 88.3,50.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 85,36.2 L 85,48.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 107.4,62.7 L 107.4,61.8 L 106.5,61.3\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 70.3,61.3 L 69.3,61.8 L 68.4,61.3\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 51.2,51.4 L 50.2,50.9 L 50.2,49.8\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 68.3,18.4 L 69.3,17.8 L 70,18.3\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003ctext x=\"122.5\" y=\"57.4\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"131.6\" y=\"57.4\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eH\u003c\/text\u003e\n\u003ctext x=\"103.5\" y=\"90.4\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"112.6\" y=\"90.4\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eH\u003c\/text\u003e\n\u003ctext x=\"121.7\" y=\"95.7\" font-size=\"8\" stroke=\"none\" fill=\"#000\"\u003e2\u003c\/text\u003e\n\u003ctext x=\"20.1\" y=\"24.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eA\u003c\/text\u003e\n\u003ctext x=\"29.2\" y=\"24.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"84.4\" y=\"35.4\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp style=\"font-size:12px;margin:4px 0 0 0;\"\u003e\n\u003cem\u003eGeneral reaction: 5-aryl-2-pyridinecarbonitrile → 5-aryl-2-pyridinecarboxamidine.\u003c\/em\u003e\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e\n\u003cstrong\u003eCross-electrophile coupling.\u003c\/strong\u003e It was the model aryl bromide in a nickel-mediated, net-reductive cross-electrophile coupling with an alkyl N-hydroxyphthalimide ester, driven by photoactive electron donor–acceptor complexes.\u003c\/p\u003e\n\u003cdiv style=\"margin:8px 0 18px 0;\"\u003e\n\u003cdiv style=\"display:flex;flex-wrap:wrap;align-items:center;justify-content:flex-start;gap:2px;\"\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"140px\" height=\"100px\" viewbox=\"0 0 140 100\"\u003e\n\u003cpath d=\"M 24,24.2 L 38.4,32.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 25.6,21.3 L 40.1,29.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 22.4,27 L 36.8,35.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 38.4,32.4 L 57.6,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 57.6,43.2 L 57.7,65.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 57.7,65.2 L 76.8,76.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 61,63.3 L 76.8,72.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 76.8,76.1 L 95.8,65\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 95.8,65 L 110.2,73.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 95.8,65 L 95.7,43\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 92.5,63.1 L 92.4,44.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 95.7,43 L 81.2,34.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 71.9,34.9 L 57.6,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 73.5,37.7 L 60.9,45.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 37.7,32 L 38.4,32.4 L 39.4,32.9\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 57.7,64.1 L 57.7,65.2 L 58.7,65.8\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 75.9,75.6 L 76.8,76.1 L 77.8,75.6\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 95.7,44.1 L 95.7,43 L 94.9,42.6\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003ctext x=\"15.4\" y=\"28.1\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"111\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eB\u003c\/text\u003e\n\u003ctext x=\"120.1\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"72.6\" y=\"38.7\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003cdiv style=\"font-size:20px;padding:0 4px;align-self:center;\"\u003e+\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"170px\" height=\"110px\" viewbox=\"0 0 170 110\"\u003e\n\u003cpath d=\"M 53.3,23.5 L 46,36.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 50.4,21.9 L 43.2,34.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 45.1,34.5 L 53.4,48.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 60.8,53.5 L 73.4,53.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 81.5,48.8 L 91,35.7\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 93,36.3 L 88.2,21.6\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 89.8,37.3 L 85,22.6\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 91,35.7 L 112,42.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 112,42.5 L 131,31.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 115.3,44.4 L 131,35.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 131,31.4 L 150.1,42.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 150.1,42.4 L 150.1,64.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 146.8,44.3 L 146.8,62.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 150.1,64.4 L 131,75.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 131,75.4 L 112,64.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 131,71.6 L 115.3,62.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 112,64.5 L 91,71.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 89.8,69.6 L 84.2,87\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 93,70.6 L 87.4,88\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 45.1,34.5 L 27.8,34.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 91,71.3 L 82.8,59.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 112,64.5 L 112,42.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 45.5,35.2 L 45.1,34.5 L 44.2,34.5\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 90.5,36.3 L 91,35.7 L 92.1,36\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 130,32 L 131,31.4 L 131.9,32\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 149.1,41.9 L 150.1,42.4 L 150.1,43.5\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 150.1,63.3 L 150.1,64.4 L 149.1,65\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 132,74.9 L 131,75.4 L 130.1,74.9\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 92.1,70.9 L 91,71.3 L 90.6,70.7\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003ctext x=\"52.1\" y=\"22\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eO\u003c\/text\u003e\n\u003ctext x=\"52.1\" y=\"60.1\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eO\u003c\/text\u003e\n\u003ctext x=\"74.1\" y=\"60.1\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"80.2\" y=\"21.4\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eO\u003c\/text\u003e\n\u003ctext x=\"80.3\" y=\"98.8\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eO\u003c\/text\u003e\n\u003ctext x=\"19.1\" y=\"41.1\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eR\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003cdiv style=\"display:flex;flex-direction:column;align-items:center;justify-content:center;min-width:90px;max-width:150px;padding:0 4px;text-align:center;font-size:12px;line-height:1.3;\"\u003e\n\u003cdiv\u003eNi catalyst,\u003c\/div\u003e\n\u003cdiv style=\"font-size:30px;line-height:1;\"\u003e⟶\u003c\/div\u003e\n\u003cdiv\u003elight\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"150px\" height=\"100px\" viewbox=\"0 0 150 100\"\u003e\n\u003cpath d=\"M 31.9,24.2 L 46.3,32.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 33.5,21.3 L 47.9,29.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 30.2,27 L 44.7,35.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 46.3,32.4 L 65.4,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 65.4,43.2 L 65.6,65.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 65.6,65.2 L 84.7,76.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 68.9,63.3 L 84.7,72.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 84.7,76.1 L 103.7,65\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 103.7,65 L 118.1,73.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 103.7,65 L 103.5,43\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 100.4,63.1 L 100.3,44.9\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 103.5,43 L 89.1,34.8\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 79.7,34.9 L 65.4,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 81.4,37.7 L 68.8,45.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 45.6,32 L 46.3,32.4 L 47.3,32.9\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 65.6,64.1 L 65.6,65.2 L 66.5,65.8\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 83.7,75.6 L 84.7,76.1 L 85.7,75.6\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 103.5,44.1 L 103.5,43 L 102.8,42.6\" stroke-miterlimit=\"10\"\u003e\u003c\/path\u003e\n\u003ctext x=\"23.2\" y=\"28.1\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"118.8\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eR\u003c\/text\u003e\n\u003ctext x=\"80.5\" y=\"38.7\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp style=\"font-size:12px;margin:4px 0 0 0;\"\u003e\n\u003cem\u003eGeneral reaction: aryl bromide + alkyl N-hydroxyphthalimide ester → 5-alkyl-2-pyridinecarbonitrile (cross-electrophile coupling).\u003c\/em\u003e\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e\n\u003cstrong\u003eTriazine formation.\u003c\/strong\u003e With ammonium bromide and diisopropylethylamine it forms 2,4,6-tris(5-bromopyridin-2-yl)-1,3,5-triazine. Palladium-catalysed coupling of this tribromide with 4-aminophenylboronic acid pinacol ester gives the matching triamine. That triamine and the matching trialdehyde are the two monomers of a triazine-based covalent organic framework.\u003c\/p\u003e\n\u003cdiv style=\"margin:8px 0 18px 0;\"\u003e\n\u003cdiv style=\"display:flex;flex-wrap:wrap;align-items:center;justify-content:flex-start;gap:2px;\"\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"140px\" height=\"100px\" viewbox=\"0 0 140 100\"\u003e\n\u003cpath d=\"M 24,24.2 L 38.4,32.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 25.6,21.3 L 40.1,29.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 22.4,27 L 36.8,35.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 38.4,32.4 L 57.6,43.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 57.6,43.2 L 57.7,65.2\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 57.7,65.2 L 76.8,76.1\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 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fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"111\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eB\u003c\/text\u003e\n\u003ctext x=\"120.1\" y=\"82.5\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"72.6\" y=\"38.7\" font-size=\"13\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003cdiv style=\"display:flex;flex-direction:column;align-items:center;justify-content:center;min-width:90px;max-width:150px;padding:0 4px;text-align:center;font-size:12px;line-height:1.3;\"\u003e\n\u003cdiv\u003eNH\u003csub\u003e4\u003c\/sub\u003eBr, \u003ci\u003ei\u003c\/i\u003ePr\u003csub\u003e2\u003c\/sub\u003eNEt\u003c\/div\u003e\n\u003cdiv style=\"font-size:30px;line-height:1;\"\u003e⟶\u003c\/div\u003e\n\u003cdiv\u003etrimerisation\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"display:flex;align-items:center;\"\u003e\n\u003csvg fill=\"none\" stroke=\"#000\" stroke-width=\"1.6\" font-family=\"sans-serif\" role=\"img\" style=\"max-width:100%;height:auto;\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"230px\" height=\"200px\" viewbox=\"0 0 230 200\"\u003e\n\u003cpath d=\"M 116.1,29.9 L 116.1,43.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 116.1,43.3 L 98.6,53.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 98.6,53.3 L 98.6,73.5\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 101.6,55.1 L 101.6,71.7\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 98.6,73.5 L 116,83.6\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 116,83.6 L 129.2,76\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 116,80.1 L 127.7,73.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 133.5,69.3 L 133.5,53.4\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 116,83.6 L 116,103.7\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 116,103.7 L 102.8,111.3\"\u003e\u003c\/path\u003e\n\u003cpath d=\"M 98.5,120.5 L 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fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"147.1\" y=\"170.3\" font-size=\"12\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003ctext x=\"18.4\" y=\"180.1\" font-size=\"12\" stroke=\"none\" fill=\"#000\"\u003eB\u003c\/text\u003e\n\u003ctext x=\"26.7\" y=\"180.1\" font-size=\"12\" stroke=\"none\" fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"59.9\" y=\"139.9\" font-size=\"12\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp style=\"font-size:12px;margin:4px 0 0 0;\"\u003e\n\u003cem\u003eReaction: 3 × 5-bromopyridine-2-carbonitrile → 2,4,6-tris(5-bromopyridin-2-yl)-1,3,5-triazine.\u003c\/em\u003e\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e\n\u003cstrong\u003eCysteine conjugation.\u003c\/strong\u003e 2-Cyanopyridines with electron-withdrawing groups react efficiently with cysteine under aqueous, mild conditions, which allows N-terminal cysteine bioconjugation. 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fill=\"#000\"\u003er\u003c\/text\u003e\n\u003ctext x=\"74.9\" y=\"50.9\" font-size=\"12\" stroke=\"none\" fill=\"#000\"\u003eN\u003c\/text\u003e\n\u003c\/svg\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cp style=\"font-size:12px;margin:4px 0 0 0;\"\u003e\n\u003cem\u003eReaction: 5-bromopyridine-2-carbonitrile + cysteine → thiazoline.\u003c\/em\u003e\n\u003c\/p\u003e\n\u003c\/div\u003e\n\u003cp\u003e\n\u003cstrong\u003eDiketopyrrolopyrrole polymers.\u003c\/strong\u003e As the monobrominated starting material, it places one bromine atom on the pyridine unit of an unsymmetric DPP, enabling a type II regioregular polymer. Pyridine-DPP is a building block for low band-gap donor copolymers in polymer solar cells.\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"margin-bottom: 28px;\"\u003e\n\u003cdiv style=\"background: #002147; padding: 10px 20px; margin-bottom: 0;\"\u003e\n\u003ch3 style=\"margin: 0; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; font-size: 0.70em; font-weight: bold; letter-spacing: 0.12em; text-transform: uppercase; color: #fff;\"\u003eShipping Destinations\u003c\/h3\u003e\n\u003c\/div\u003e\n\u003cdiv style=\"border: 1px solid #e4e8f0; border-top: none; padding: 12px 16px; font-family: 'Helvetica Neue', Helvetica, Arial, sans-serif; font-size: 0.95em;\"\u003e\n\u003cul style=\"margin: 0; padding: 0; list-style: none;\"\u003e\n\u003cli style=\"padding: 5px 0; border-bottom: 1px solid #f0f0f0;\"\u003e\n\u003cspan style=\"display: inline-block; width: 7px; height: 7px; background: #002147; border-radius: 50%; margin-right: 10px; vertical-align: middle;\"\u003e\n\u003c\/span\u003eEU \u0026amp; UK: Priority delivery, 2–5 business days.\u003c\/li\u003e\n\u003cli style=\"padding: 5px 0; border-bottom: 1px solid #f0f0f0;\"\u003e\n\u003cspan style=\"display: inline-block; width: 7px; height: 7px; background: #002147; border-radius: 50%; margin-right: 10px; vertical-align: middle;\"\u003e\n\u003c\/span\u003eUnited States (DDP): 3–7 business days, duties and taxes prepaid.\u003c\/li\u003e\n\u003cli style=\"padding: 5px 0; border-bottom: 1px solid #f0f0f0;\"\u003e\n\u003cspan style=\"display: inline-block; width: 7px; height: 7px; background: #002147; border-radius: 50%; margin-right: 10px; vertical-align: middle;\"\u003e\n\u003c\/span\u003eEFTA Countries (DDP): 3–7 business days, duties and taxes prepaid.\u003c\/li\u003e\n\u003cli style=\"padding: 5px 0; border-bottom: 1px solid #f0f0f0;\"\u003e\n\u003cspan style=\"display: inline-block; width: 7px; height: 7px; background: #002147; border-radius: 50%; margin-right: 10px; vertical-align: middle;\"\u003e\n\u003c\/span\u003eWorldwide: 7–14 business days, selected locations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"NorrChemica™","offers":[{"title":"5.0 g","offer_id":55186828329297,"sku":"NOR-97483777-5g","price":64.2,"currency_code":"EUR","in_stock":true},{"title":"10 g","offer_id":55186828362065,"sku":"NOR-97483777-10g","price":79.2,"currency_code":"EUR","in_stock":true},{"title":"25 g","offer_id":55186828394833,"sku":"NOR-97483777-25g","price":98.2,"currency_code":"EUR","in_stock":true},{"title":"50 g","offer_id":55257502220625,"sku":"NOR-97483777-50g","price":149.2,"currency_code":"EUR","in_stock":false},{"title":"100 g","offer_id":55257502253393,"sku":"NOR-97483777-100g","price":249.2,"currency_code":"EUR","in_stock":false},{"title":"250 g","offer_id":55257502286161,"sku":"NOR-97483777-250g","price":498.2,"currency_code":"EUR","in_stock":false},{"title":"500 g","offer_id":55257502318929,"sku":"NOR-97483777-500g","price":849.2,"currency_code":"EUR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0954\/6357\/1793\/files\/5-Bromopyridine-2-carbonitrile.png?v=1791719798","url":"https:\/\/www.norrchemica.com\/products\/5-bromopyridine-2-carbonitrile-cas-97483-77-7","provider":"NorrChemica","version":"1.0","type":"link"}