60480-06-0

Basic information

• Product Name: 2-chloroethyl (4-nitrophenyl)carbamate
• CAS NO: 60480-06-0
• Molecular Formula: C₉H₉ClN₂O₄
• Molecular Weight: 244.6318
• Mol File: 60480-06-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 340.6°C at 760 mmHg
• Flash Point: 159.8°C
• Density: 1.45g/cm³
• Vapor Pressure: 8.49E-05mmHg at 25°C
• Refractive Index: 1.607
• CAS DataBase Reference: 2-chloroethyl (4-nitrophenyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloroethyl (4-nitrophenyl)carbamate(60480-06-0)
• EPA Substance Registry System: 2-chloroethyl (4-nitrophenyl)carbamate(60480-06-0)

Safety Data

• Hazardous Substances Data: 60480-06-0(Hazardous Substances Data)

Upstream product

• 627-11-2 2-Chloroethyl chloroformate 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 20403-78-5 2-methyl-3-oxo-cyclopentanecarboxylic acid 4-(2-oxo-oxazolidin-3-yl)-anilide 
• 22036-37-9 3-{4-[bis-(2-chloro-ethyl)-amino]-phenyl}-oxazolidin-2-one 
• 22036-36-8 3-{4-[bis-(2-hydroxy-ethyl)-amino]-phenyl}-oxazolidin-2-one 
• 20403-48-9 N-[4-(2-oxo-oxazolidin-3-yl)-phenyl]-phthalimide 
• 20403-77-4 [4-(2-oxo-oxazolidin-3-yl)-phenyl]-carbamic acid 2-chloro-ethyl ester 
• 20406-71-7 3-[4-(2,2-dichloro-acetylamino)-phenyl]-oxazolidin-2-one 
• 20406-73-9 [4-(2-oxo-oxazolidin-3-yl)-phenyl]-carbamic acid ethyl ester 
• 20406-72-8 3-[4-(2-chloro-acetylamino)-phenyl]-oxazolidin-2-one 
• 22036-26-6 3-(4-aminophenyl)-1,3-oxazolidin-2-one 
• 31847-21-9 3-(3-{4-[bis-(2-chloro-ethyl)-amino]-2-methyl-benzylideneamino}-phenyl)-oxazolidin-2-one 
• 31847-20-8 3-(3-{4-[bis-(2-chloro-ethyl)-amino]-benzylideneamino}-phenyl)-oxazolidin-2-one 
• 34232-43-4 3-(3-aminophenyl)oxazolidin-2-one 
• 20403-49-0 N,O-Bis-dichloracetyl-N-<4-nitro-phenyl>-aethanolamin 
• 20403-50-3 N,O-Bis-chloracetyl-N-<4-nitro-phenyl>-aethanolamin 

Relevant articles and documents

Short and practical synthesis of N′,N′-disubstituted N-aryl-1,2-ethylene-diamines by a decarboxylative ring-opening reaction under nucleophilic conditions

A straightforward and practical synthesis of N′,N′- disubstituted N-aryl-1,2-ethylenediamines, starting from anilines, via N-aryloxazolidin-2-ones is described. A decarboxylative ring-opening reaction of N-aryloxazolidin-2-ones, using aliphatic secondary