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

• Catalog No.: 94624
• CAS Number: 212333-72-7
• M. F.: C10H16F6N3OPS
• M. W.: 371.2827202
• Purity: ≥95.0% (NMR)

SYNONYMS

• Title: S-(1-氧代-2-吡啶基)-N,N,N′,N′-四甲基硫脲六氟磷酸盐
• IUPAC name: hexafluoro-λ^5-phosphanuide 2-{[bis(dimethylamino)methylidene]-λ^4-sulfanyliumyl}pyridin-1-ium-1-olate
• IUPAC Traditional name: 2-{[bis(dimethylamino)methylidene]-λ^4-sulfanyliumyl}pyridin-1-ium-1-olate hexafluorophosphate
• Synonyms: N,N,N′,N′-四甲基-S-(1-氧代-2-吡啶基)硫脲六氟磷酸盐; S-(2-吡啶基)-N,N,N′,N′-四甲基硫脲 N-氧化物六氟磷酸盐; N,N,N′,N′-Tetramethyl-S-(1-oxido-2-pyridyl)thiuronium hexafluorophosphate; S-(2-Pyridyl)-N,N,N′,N′-tetramethylthiuronium N-oxide hexafluorophosphate

DATABASE IDS

• CAS Number: 212333-72-7
• MDL Number: MFCD05865266
• PubChem SID: 24890030

PROPERTIES

• Empirical Formula (Hill Notation): C10H16F6N3OPS
• Purity: ≥95.0% (NMR)
• Melting Point: 120-125 °C
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• Storage Temperature: -20°C
• German water hazard class: 3

DETAILS

Description (English)

Other Notes
Very reactive peptide coupling reagent7,5
Packaging
5, 25 g in glass bottle
Application
Reagent for: Synthesis of inhibitors for PAD1, 3, and 41 Synthesis of enantiomerically pure vinylcyclopropylboronic esters2 Synthesis of enantiomerically pure cyclopropane building blocks3 Camphor-derived chiral auxiliary for hydroxyalkyl radicals4 Solution and solid-phase coupling5 Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides6

Description (简体中文)

Other Notes
非常活泼的肽偶联试剂7,5
包装
5, 25 g in glass bottle
Application
Reagent for: Synthesis of inhibitors for PAD1, 3, and 41 Synthesis of enantiomerically pure vinylcyclopropylboronic esters2 Synthesis of enantiomerically pure cyclopropane building blocks3 Camphor-derived chiral auxiliary for hydroxyalkyl radicals4 Solution and solid-phase coupling5 Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides6