90656-49-8

Basic information

• Product Name: Benzoic acid, 2-[(3-chlorophenyl)amino]-5-nitro-
• CAS NO: 90656-49-8
• Molecular Formula: C13H9ClN2O4
• Molecular Weight: 292.678
• Mol File: 90656-49-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-[(3-chlorophenyl)amino]-5-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-[(3-chlorophenyl)amino]-5-nitro-(90656-49-8)
• EPA Substance Registry System: Benzoic acid, 2-[(3-chlorophenyl)amino]-5-nitro-(90656-49-8)

Safety Data

• Hazardous Substances Data: 90656-49-8(Hazardous Substances Data)

Upstream product

• 2516-96-3 2-chloro-5-nitrobenzoic acid 
• 108-42-9 3-chloro-aniline 

Downstream Products

• 860536-64-7 (4-bromo-phenyl)-(1-chloro-7-nitro-acridin-9-yl)-amine 
• 731817-60-0 2-(3-chloro-anilino)-5-nitro-benzoyl chloride 
• 23045-21-8 8-chloro-acridin-2-ylamine 
• 40505-20-2 3-Amino-8-chloroacridin 

Relevant articles and documents

Metal catalyst-free amination of 2-chloro-5-nitrobenzoic acid in superheated water

A series of N-arylanthranilic acid derivatives were synthesised by amination of 2-chloro-5-nitrobenzoic acid with various arylamine in superheated water with potassium carbonate as base. Good yields were achieved within 2-3 h at 150-190 °C. The results indicated that this metal catalyst-free method is a simple, environmentally-friendly and efficient synthesis of N-phenylanthranilic acid derivatives. Furthermore, it will work with an alkylamine and phenol.

Catalyst-free microwave-assisted amination of 2-chloro-5-nitrobenzoic acid

(Chemical Equation Presented) The synthesis of N-substituted 5-nitroanthranilic acid derivatives 3a-w was achieved by a new, mild, microwave-assisted, regioselective amination reaction of 5-nitro-2-chlorobenzoic acid (1a) with a diverse range of aliphatic