94624

S-(1-Oxido-2-pyridyl)-N,N,N′,N′-tetramethylthiuronium hexafluorophosphate

≥95.0% (NMR)

• Sinónimos: N,N,N′,N′-Tetramethyl-S-(1-oxido-2-pyridyl)thiuronium hexafluorophosphate, S-(2-Pyridyl)-N,N,N′,N′-tetramethylthiuronium N-oxide hexafluorophosphate
• Fórmula empírica (notación de Hill): C₁₀H₁₆F₆N₃OPS
• Número de CAS: 212333-72-7
• Peso molecular: 371.28
• MDL number: MFCD05865266
• UNSPSC Code: 12352101
• PubChem Substance ID: 57653626
• NACRES: NA.22

Propiedades

• assay: ≥95.0% (NMR)
• form: crystals
• reaction suitability: reaction type: Coupling Reactions
• mp: 120-125 °C
• application(s): peptide synthesis
• functional group: amine; thiourea
• storage temp.: −20°C
• SMILES string: F[P-](F)(F)(F)(F)F.CN(C)\C(=[S+]\c1cccc[n+]1[O-])N(C)C
• InChI: 1S/C10H16N3OS.F6P/c1-11(2)10(12(3)4)15-9-7-5-6-8-13(9)14;1-7(2,3,4,5)6/h5-8H,1-4H3;/q+1;-1
• InChI key: UCOGEMMJHLHOAW-UHFFFAOYSA-N

Descripción

Application

Reagent for:
Synthesis of inhibitors for PAD1, 3, and 4
Synthesis of enantiomerically pure vinylcyclopropylboronic esters
Synthesis of enantiomerically pure cyclopropane building blocks
Camphor-derived chiral auxiliary for hydroxyalkyl radicals
Solution and solid-phase coupling
Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides

Other Notes

Very reactive peptide coupling reagent[1][2]

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)