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    NorrChemica — Chemicals & Analysis, Helsinki
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    • Chemical structure of Cesium Carbonate (anhydrous), Cs₂CO₃, CAS 534-17-8, ≥99% — mild inorganic base widely used in palladium-catalysed cross-couplings (Suzuki-Miyaura, Buchwald-Hartwig), N- and O-alkylation reactions, and selective deprotonation in organic synthesis. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.​​​​​​​​​​​​​​​​

      Cesium Carbonate | CAS 534-17-8 | ≥99%

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      Cesium CarbonateCAS 534-17-8 · ≥99%

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    • Chemical structure of GMBS (N-succinimidyl 4-maleimidobutyrate), CAS 80307-12-6, ≥98% — a heterobifunctional crosslinker (C12H12N2O6): an amine-reactive NHS ester and a thiol-reactive maleimide on a short aliphatic butyryl spacer. The NHS ester couples to amines and the maleimide to thiols in a two-step conjugation; its aliphatic arm is less immunogenic than aromatic or cyclohexane crosslinkers, favoring hapten-carrier immunogens and enzyme-antibody conjugates. Supplied by NorrChemica with DDP shipping. CoA

      GMBS | CAS 80307-12-6 | ≥98%

      GMBSCAS 80307-12-6 · ≥98%

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    • Chemical structure of (R)-BINAP ((R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl), CAS 76189-55-4, ≥99% — C2-symmetric, axially chiral (atropisomeric) bisphosphine ligand (C44H32P2), a 1,1'-binaphthyl backbone bearing a diphenylphosphino (PPh2) group at the 2 and 2' positions. The (R) antipode of (S)-BINAP, a landmark ligand for metal-catalyzed asymmetric hydrogenation (Ru/Rh-BINAP) and enantioselective catalysis. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      (R)-BINAP | CAS 76189-55-4 | ≥99%

      (R)-BINAPCAS 76189-55-4 · ≥99%

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    • Chemical structure of (S)-1,1'-Bi-2-naphthol ((S)-(-)-BINOL), CAS 18531-99-2, ≥98% — C2-symmetric, axially chiral (atropisomeric) binaphthol (C20H14O2), two naphthalene units joined at the 1,1'-positions bearing hydroxyl groups at 2 and 2'. The (S) antipode of (R)-BINOL, a privileged chiral diol ligand and organocatalyst precursor for asymmetric synthesis, from BINOL-metal Lewis acids to chiral phosphoric acids. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      (S)-1,1′-Bi-2-naphthol | CAS 18531-99-2 | ≥98%

      (S)-1,1′-Bi-2-naphtholCAS 18531-99-2 · ≥98%

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    • Chemical structure of 2′-Deoxyguanosine monohydrate (dG, C₁₀H₁₅N₅O₅), CAS 312693-72-4, ≥97% — the 2′-deoxyribonucleoside of guanine, converted by kinases to dGTP, the substrate of DNA polymerases. Used as a nucleoside supplement in cell culture, in research on deoxyguanosine kinase and mitochondrial DNA, to deplete thymocytes from thymic lobes in organ culture, and in studies of oxidative damage to DNA. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      2′-Deoxyguanosine monohydrate | CAS 312693-72-4 | ≥97%

      2′-Deoxyguanosine monohydrateCAS 312693-72-4 · ≥97%

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    • Chemical structure of Copper(II) Acetate Monohydrate (Cu(OAc)₂·H₂O), CAS 6046-93-1, ≥98% — blue-green copper carboxylate used stoichiometrically as the oxidant and copper source in Chan–Lam C–N and C–O coupling of boronic acids with amines and phenols, and as a Lewis-acidic copper(II) source in oxidative and aerobic transformations. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      Copper(II) Acetate Monohydrate (Cu(OAc)2·H2O) | CAS 6046-93-1 | ≥98%

      Copper(II) Acetate Monohydrate (Cu(OAc)2·H2O)CAS 6046-93-1 · ≥98%

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    • Chemical structure of Pseudouridine (Ψ, 5-ribosyluracil, C₉H₁₂N₂O₆), CAS 1445-07-4, ≥98% — C-nucleoside isomer of uridine with the ribose bound to C5 of uracil, and the most common modified nucleoside in RNA. Used in research on RNA modification and on pseudouridine-containing mRNA, which has a higher translational capacity and lower immunogenicity, in mapping pseudouridine by CMC and bisulfite sequencing, and as a kidney function marker. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      Pseudouridine | CAS 1445-07-4 | ≥98%

      PseudouridineCAS 1445-07-4 · ≥98%

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    • Chemical structure of 2-Fluoropyridine-5-boronic Acid, CAS 351019-18-6, ≥98% — heteroaromatic pyridyl boronic acid used in Pd-catalysed Suzuki-Miyaura coupling, Cu Chan-Lam C–N/C–O coupling, Rh/Ni conjugate additions, and photoredox arylation in pharma/materials synthesis, with the 2-fluoropyridine handle valuable for SNAr displacement by amines, alkoxides, and thiolates in medicinal chemistry pyridine SAR. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      2-Fluoropyridine-5-boronic Acid | CAS 351019-18-6 | ≥98%

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      2-Fluoropyridine-5-boronic AcidCAS 351019-18-6 · ≥98%

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    • Chemical structure of PyFluor (pyridine-2-sulfonyl fluoride), C₅H₄FNO₂S, CAS 878376-35-3, ≥97% — thermally stable deoxyfluorination reagent converting primary and secondary alcohols to alkyl fluorides with a guanidine or amidine base, developed as a selective alternative to DAST with minimal elimination byproducts. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      PyFluor (Pyridine-2-sulfonyl Fluoride) | CAS 878376-35-3 | ≥97%

      PyFluor (Pyridine-2-sulfonyl Fluoride)CAS 878376-35-3 · ≥97%

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    • Chemical structure of Schreiner's Thiourea Catalyst (1,3-bis[3,5-bis(trifluoromethyl)phenyl]thiourea), CAS 1060-92-0, ≥98% — a thiourea flanked by two 3,5-bis(trifluoromethyl)phenyl groups (C17H8F12N2S); the four CF3 groups acidify its N-H protons into a strong double hydrogen-bond donor. The archetypal achiral hydrogen-bond-donor organocatalyst, it activates carbonyls, nitroalkenes and imines, as exploited in Schreiner's acid-free acetalization of aldehydes. Supplied by NorrChemica with DDP shipping. CoA

      Schreiner’s Thiourea Catalyst | CAS 1060-92-0 | ≥98%

      Schreiner’s Thiourea CatalystCAS 1060-92-0 · ≥98%

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    • Chemical structure of D-Proline, CAS 344-25-2 — the (R)-enantiomer of the cyclic amino acid proline, used as an organocatalyst and chiral building block in asymmetric synthesis and peptide chemistry. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      D-Proline | CAS 344-25-2 | ≥98%

      D-ProlineCAS 344-25-2 · ≥98%

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    • Chemical structure of CyJohnPhos (2-(dicyclohexylphosphino)biphenyl; (2-biphenyl)dicyclohexylphosphine), CAS 247940-06-3, ≥98% — bulky, electron-rich, air-stable monodentate dialkylbiaryl (Buchwald) phosphine ligand (C24H31P), a dicyclohexylphosphino group at the 2-position of a biphenyl scaffold. A highly active ligand for Pd-catalyzed Buchwald-Hartwig amination and Suzuki coupling of aryl chlorides, and for gold(I) catalysis. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      CyJohnPhos | CAS 247940-06-3 | ≥98%

      CyJohnPhosCAS 247940-06-3 · ≥98%

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    • Chemical structure of SPhos (2-dicyclohexylphosphino-2',6'-dimethoxybiphenyl), CAS 657408-07-6, ≥98% — an air-stable, electron-rich dialkylbiaryl phosphine ligand (C26H35O2P) developed by the Buchwald group. A rationally designed universal ligand for Pd-catalyzed Suzuki-Miyaura coupling, excelling with aryl chlorides, hindered biaryls and heterobiaryls; also used in Buchwald-Hartwig C-N amination and Negishi coupling. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      SPhos | CAS 657408-07-6 | ≥98%

      SPhosCAS 657408-07-6 · ≥98%

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    • Chemical structure of D-Cycloserine ((R)-4-amino-1,2-oxazolidin-3-one), CAS 68-41-7, ≥98% — cyclic analogue of D-alanine that inhibits alanine racemase and D-alanyl-D-alanine ligase in bacterial peptidoglycan synthesis, used as the selective agent in cycloserine–cefoxitin fructose agar for isolating Clostridioides difficile and as an NMDA-receptor glycine-site partial agonist in neuroscience research. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      D-Cycloserine | CAS 68-41-7 | ≥98%

      D-CycloserineCAS 68-41-7 · ≥98%

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    • Chemical structure of (S)-BINAP ((S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl), CAS 76189-56-5, ≥99% — C2-symmetric, axially chiral (atropisomeric) bisphosphine ligand (C44H32P2), a 1,1'-binaphthyl backbone bearing a diphenylphosphino (PPh2) group at the 2 and 2' positions, its chirality arising from restricted rotation about the binaphthyl axis. A landmark ligand for metal-catalyzed asymmetric hydrogenation (Ru/Rh-BINAP) and enantioselective catalysis. Supplied by NorrChemica with DDP shipping. CoA

      (S)-BINAP | CAS 76189-56-5 | ≥99%

      (S)-BINAPCAS 76189-56-5 · ≥99%

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    • Chemical structure of BrettPhos (2-(dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-triisopropyl-1,1'-biphenyl), CAS 1070663-78-3, ≥97% — a bulky, electron-rich dialkylbiaryl phosphine ligand (C35H53O2P) developed by the Buchwald group. A premier ligand for Pd-catalyzed Buchwald-Hartwig C-N amination, best known for selective monoarylation of primary amines and for coupling aryl chlorides and mesylates; also used in Pd-catalyzed aromatic fluorination. Supplied by NorrChemica with DDP shipping. CoA and SDS.

      BrettPhos | CAS 1070663-78-3 | ≥97%

      BrettPhosCAS 1070663-78-3 · ≥97%

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    • Chemical structure of XPhos Pd G3, CAS 1445085-55-1, ≥98% — a third-generation Buchwald aminobiphenyl palladacycle carrying the bulky XPhos ligand, which on base activation releases the monoligated LPd(0) active species, used for Buchwald-Hartwig amination, Suzuki-Miyaura coupling and C-N bond formation with hindered or heteroaryl partners. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      XPhos Pd G3 | CAS 1445085-55-1 | ≥98%

      XPhos Pd G3CAS 1445085-55-1 · ≥98%

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    • Chemical structure of Copper(I) Iodide (cuprous iodide; copper monoiodide), CAS 7681-65-4, ≥99% — inorganic copper(I) salt (CuI), copper in the +1 oxidation state with iodide (Cu+ and I-). A widely used catalyst and co-catalyst: the classic copper(I) co-catalyst with palladium in Sonogashira coupling, and a catalyst for Ullmann-type C-N/C-O/C-S coupling, N-arylation and click (CuAAC) chemistry; also a p-type semiconductor for thin-film devices. Supplied by NorrChemica with DDP shipping. CoA and SDS provided

      Copper(I) Iodide | CAS 7681-65-4 | ≥99%

      Copper(I) IodideCAS 7681-65-4 · ≥99%

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    • Chemical structure of D-Phenylalanine, CAS 673-06-3, ≥99.0% — unnatural D-enantiomer of phenylalanine used as a chiral building block in peptide synthesis, asymmetric catalysis, and enantioselective biotransformation studies. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.​​​​​​​​​​​​​​​​

      D-Phenylalanine | CAS 673-06-3 | ≥99%

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      D-PhenylalanineCAS 673-06-3 · ≥99%

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    • Chemical structure of D-Tartaric Acid, CAS 147-71-7, ≥99.0% — (2S,3S)-(−)-tartaric acid, an enantiopure chiral-pool building block and resolving agent for asymmetric synthesis, optical resolution of racemic amines, and preparation of chiral tartrate ligands and catalysts. Supplied by NorrChemica with DDP shipping. CoA and SDS provided.

      D-Tartaric Acid | CAS 147-71-7 | ≥99.0%

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      D-Tartaric AcidCAS 147-71-7 · ≥99.0%

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