64392-59-2

Basic information

• Product Name: Carbamic acid, [(2-aminophenyl)methyl]-, phenylmethyl ester
• CAS NO: 64392-59-2
• Molecular Formula: C15H16N2O2
• Molecular Weight: 256.304
• Mol File: 64392-59-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [(2-aminophenyl)methyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [(2-aminophenyl)methyl]-, phenylmethyl ester(64392-59-2)
• EPA Substance Registry System: Carbamic acid, [(2-aminophenyl)methyl]-, phenylmethyl ester(64392-59-2)

Safety Data

• Hazardous Substances Data: 64392-59-2(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 4403-69-4 2-amino-1-benzylamine 
• 13795-24-9 benzyl 4-nitrophenyl carbonate 
• 1885-29-6 anthranilic acid nitrile 

Downstream Products

• 1244783-42-3 2-Boc-aminobenzyl-Cbz-amine 
• 1242190-89-1 N-[(2-N'-benzyloxycarbonylaminomethyl)phenyl]-4-pentyamide 
• 64392-60-5 o-(N'-Formylamino)-N-carbobenzyloxybenzylamin 

Relevant articles and documents

A versatile PIFA-mediated approach to structurally diverse pyrrolo(benzo)diazepines from linear alkynylamides

The addition of the hypervalent iodine reagent PIFA [phenyliodine(III) bis(trifluoroacetate)] to a series of properly substituted N-(3-aminopropyl) alkynylamides results in the efficient formation of a functionalized 5-aroyl-2-pyrrolidinone skeleton. By p

Study of biscarbamates derived from 2-aminobenzylamines as models for alcohol prodrugs

Unsubstituted N-arylcarbamate of title compound does not cyclize to the corresponding cyclic urea, with ROH liberation, under mild conditions (40°C). Substitution of the benzylic position by two methyl groups promotes slow cyclisation while N-methylation