Substance
ID:321027
Names and Identifiers
IUPAC name
tert-butyl N-[2-(aminomethyl)phenyl]carbamate
IUPAC Traditional name
tert-butyl N-[2-(aminomethyl)phenyl]carbamate
Synonyms
tert-Butyl N-(2-aminomethylphenyl)carbamate(2-Aminomethyl-phenyl)-carbamic acid tert-butyl ester2-(Boc-氨基)苄胺2-(Boc-amino)benzylamine(2-氨甲基-苯基)-氨基甲酸叔丁酯
Properties
Product Information
Empirical Formula (Hill Notation)
C12H18N2O2
Safety Information
European Hazard Symbols
Harmful (Xn)MSDS Link
Safety Statements
36/37
GHS Hazard statements
H302-H317
GHS Precautionary statements
P280
GHS Signal Word
Warning
Risk Statements
22-43
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
German water hazard class
3
Physical Property
Flash Point
71 °C
159.8 °F
Boiling Point
238-242 °C
Density
1.054 g/mL at 25 °C
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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