tert-Butyl 2-(aminomethyl)phenylcarbamate

CAS No.：849020-94-6

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This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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tert-Butyl 2-(aminomethyl)phenylcarbamate Basic information

Product Name:	tert-Butyl 2-(aminomethyl)phenylcarbamate
Synonyms:	2-(Aminomethyl)aniline, 1-BOC protected;2-[(tert-Butoxycarbonyl)amino]benzylamine, tert-Butyl [2-(aminomethyl)phenyl]carbamate;tert-Butyl N-[2-(aminomethyl)phenyl]carbamate;2-(tert-Butoxycarbonylamino)benzylamine;2-(Boc-amino)benzylamine;2-(Aminomethyl)-N-Boc-aniline;TERT-BUTYL 2-(AMINOMETHYL)PHENYLCARBAMATE;ert-Butyl N-(2-aminomethylphenyl)carbamate
CAS:	849020-94-6
MF:	C12H18N2O2
MW:	222.28
EINECS:
Product Categories:	Building Blocks;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Polyamines;Protected Amines
Mol File:	849020-94-6.mol

tert-Butyl 2-(aminomethyl)phenylcarbamate Chemical Properties

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)

Safety Information

Hazard Codes	Xn
Risk Statements	22-43
Safety Statements	36/37
RIDADR	NA 1993 / PGIII
WGK Germany	3
HS Code	2921490090

MSDS Information

tert-Butyl 2-(aminomethyl)phenylcarbamate Usage And Synthesis

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)
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

tert-Butyl 2-(aminomethyl)phenylcarbamate Preparation Products And Raw materials

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