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2-(Boc-amino)benzylamine_Molecular_structure_CAS_849020-94-6)
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2-(Boc-amino)benzylamine

Catalog No. 709700 Name Sigma Aldrich
CAS Number 849020-94-6 Website http://www.sigmaaldrich.com
M. F. C12H18N2O2 Telephone 1-800-521-8956
M. W. 222.28352 Fax
Purity Email
Storage Chembase ID: 12224

SYNONYMS

Title
2-(Boc-氨基)苄胺
IUPAC name
tert-butyl N-[2-(aminomethyl)phenyl]carbamate
IUPAC Traditional name
tert-butyl N-[2-(aminomethyl)phenyl]carbamate
Synonyms
(2-Aminomethyl-phenyl)-carbamic acid tert-butyl ester
(2-氨甲基-苯基)-氨基甲酸叔丁酯
tert-Butyl N-(2-aminomethylphenyl)carbamate

DATABASE IDS

MDL Number MFCD04037902
CAS Number 849020-94-6

PROPERTIES

Empirical Formula (Hill Notation) C12H18N2O2
Boiling Point 238-242 °C
Density 1.054 g/mL at 25 °C
Flash Point 71 °C
Flash Point 159.8 °F
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302-H317
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
GHS Precautionary statements P280
Risk Statements 22-43
Safety Statements 36/37
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
Application
Reactant for:
• Two-step syntheses of fused quinoxaline-benzodiazepines and bis-benzodiazepines employing a double UDC (Ugi/Deprotect/Cyclize) strategy1
• Preparation of hydroquinazoline scaffolds via microwave-promoted Ugi reaction and cyclization2
• Preparation of pyrazinone inhibitors of mast cell tryptase3
Description (简体中文)
包装
1 g in glass bottle
Application
Reactant for:
• Two-step syntheses of fused quinoxaline-benzodiazepines and bis-benzodiazepines employing a double UDC (Ugi/Deprotect/Cyclize) strategy1
• Preparation of hydroquinazoline scaffolds via microwave-promoted Ugi reaction and cyclization2
• Preparation of pyrazinone inhibitors of mast cell tryptase3

REFERENCES