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S-(1-Oxido-2-pyridyl)-N,N,N′,N′-tetramethylthiuronium tetrafluoroborate_Molecular_structure_CAS_255825-38-8)
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S-(1-Oxido-2-pyridyl)-N,N,N′,N′-tetramethylthiuronium tetrafluoroborate

Catalog No. 94623 Name Sigma Aldrich
CAS Number 255825-38-8 Website http://www.sigmaaldrich.com
M. F. C10H16BF4N3OS Telephone 1-800-521-8956
M. W. 313.1231528 Fax
Purity ≥95.0% (NMR) Email
Storage Chembase ID: 152022

SYNONYMS

Title
S-(1-氧代-2-吡啶基)-N,N,N′,N′-四甲基硫脲四氟硼酸盐
IUPAC name
tetrafluoroboranuide 2-{[(dimethylamino)(dimethyliminiumyl)methyl]sulfanyl}pyridin-1-ium-1-olate
IUPAC Traditional name
2-{[(dimethylamino)(dimethyliminio)methyl]sulfanyl}pyridin-1-ium-1-olate tetrafluoroborate
Synonyms
N,N,N′,N′-Tetramethyl-S-(1-oxido-2-pyridyl)thiuronium tetrafluoroborate
S-(2-Pyridyl)-N,N,N′,N′-tetramethylthiuronium N-oxide tetrafluoroborate
S-(2-吡啶基)-N,N,N′,N′-四甲基硫脲 N-氧化物四氟硼酸盐
N,N,N′,N′-四甲基-S-(1-氧代-2-吡啶基)硫脲四氟硼酸盐

DATABASE IDS

MDL Number MFCD05664718
CAS Number 255825-38-8
PubChem SID 24890029

PROPERTIES

Empirical Formula (Hill Notation) C10H16BF4N3OS
Purity ≥95.0% (NMR)
Melting Point 109-114 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Other Notes
Very reactive peptide coupling reagent3,2
Packaging
5, 25 g in poly bottle
Application
Reagent for: Synthesis of anticonvulsants1 Solution and solid-phase peptide coupling2,3 Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides4 Rapid and high-yielding preparation of primary amides5,3
Description (简体中文)
Other Notes
非常活泼的肽偶联试剂3,2
包装
5, 25 g in poly bottle
Application
Reagent for: Synthesis of anticonvulsants1 Solution and solid-phase peptide coupling2,3 Conversion of carboxylic acids to Weinreb amides and N-methoxy or N-benzoxy amides4 Rapid and high-yielding preparation of primary amides5,3

REFERENCES