303158-02-3

Basic information

• Product Name: Carbamic acid, (4-nitrosophenyl)-, 1-methylethyl ester
• CAS NO: 303158-02-3
• Molecular Formula: C10H12N2O3
• Molecular Weight: 208.217
• Mol File: 303158-02-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (4-nitrosophenyl)-, 1-methylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (4-nitrosophenyl)-, 1-methylethyl ester(303158-02-3)
• EPA Substance Registry System: Carbamic acid, (4-nitrosophenyl)-, 1-methylethyl ester(303158-02-3)

Safety Data

• Hazardous Substances Data: 303158-02-3(Hazardous Substances Data)

Upstream product

• 122-42-9 carbamic acid, phenyl-, 1-methylethyl ester 

Downstream Products

• 14357-51-8 isopropyl N-(4-nitrophenyl)carbamate 
• 30694-25-8 N-(4-aminophenyl)carbamic acid isopropyl ester 

Relevant articles and documents

Synthesis of alkyl N-(C-nitrosoaryl)carbamates and some reactions thereof

Reactions of alkyl N-phenylcarbamates, m-di(methoxycarboxyamido)benzene, and methyl N-(o-tolyl)carbamate with nitrosylsulfuric acid in glacial acetic acid afford N-(C-nitrosoaryl)carbamates; under these conditions tert-bulyl N-phenylcarbamate suffers decarboxylation, methyl N-(p-tolyl)-, methyl N-(p-methoxyphenyl)carbamates, o-and p-di(methoxycarboxyamido)benzenes are nitrated, and isomeric methyl N-nitrophenylcarbamates and methyl N-(p-bromophenyl)carbamate do not react. The reduction of N-(C-nitrosoaryl)carbamates with dithionite afforded the corresponding aminocarbamates; the oxidation with nitric acid yielded carbamate nitro derivatives; the condensation with aniline and benzylpyridinium chloride resulted in carbamate derivatives of azobenzene and phenylnitron.