Identification | Back Directory | [Name]
tert-Butyl 2-(aminomethyl)phenylcarbamate | [CAS]
849020-94-6 | [Synonyms]
2-(Boc-amino)benzylamine 2-(Aminomethyl)-N-Boc-aniline 2-(Aminomethyl)aniline, 1-BOC protected 2-(tert-Butoxycarbonylamino)benzylamine TERT-BUTYL 2-(AMINOMETHYL)PHENYLCARBAMATE ert-Butyl N-(2-aminomethylphenyl)carbamate 2-(Aminomethyl)aniline, 1-BOC protected 95+% tert-Butyl N-[2-(aminomethyl)phenyl]carbamate tert-Butyl 2-(aminomethyl)phenylcarbamate ISO 9001:2015 REACH Carbamic acid, N-[2-(aminomethyl)phenyl]-, 1,1-dimethylethyl ester 2-[(tert-Butoxycarbonyl)amino]benzylamine, tert-Butyl [2-(aminomethyl)phenyl]carbamate | [Molecular Formula]
C12H18N2O2 | [MDL Number]
MFCD04037902 | [MOL File]
849020-94-6.mol | [Molecular Weight]
222.28 |
Chemical Properties | Back Directory | [Boiling point ]
238-242℃ | [density ]
1.054g/mLat 25℃ | [Fp ]
71°C | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [pka]
13.67±0.70(Predicted) |
Hazard Information | Back Directory | [Uses]
Reactant for:
- Two-step syntheses of fused quinoxaline-benzodiazepines and bis-benzodiazepines employing a double UDC (Ugi/Deprotect/Cyclize) strategy
- Preparation of hydroquinazoline scaffolds via microwave-promoted Ugi reaction and cyclization
- Preparation of pyrazinone inhibitors of mast cell tryptase
| [Uses]
Tert-Butyl 2-(aminomethyl)phenylcarbamate can be used as reactant for Two-step syntheses of fused quinoxaline-benzodiazepines and bis-benzodiazepines employing a double UDC (Ugi/Deprotect/Cyclize)
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Company Name: |
Energy Chemical
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Tel: |
021-021-58432009 400-005-6266 |
Website: |
http://www.energy-chemical.com |
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