32305-23-0

Basic information

• Product Name: Benzoic acid, 4-chloro-2-[(2-methoxyphenyl)amino]-
• CAS NO: 32305-23-0
• Molecular Formula: C14H12ClNO3
• Molecular Weight: 277.707
• Mol File: 32305-23-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-chloro-2-[(2-methoxyphenyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-chloro-2-[(2-methoxyphenyl)amino]-(32305-23-0)
• EPA Substance Registry System: Benzoic acid, 4-chloro-2-[(2-methoxyphenyl)amino]-(32305-23-0)

Safety Data

• Hazardous Substances Data: 32305-23-0(Hazardous Substances Data)

Upstream product

• 50-84-0 2,4 dichlorobenzoic acid 
• 90-04-0 2-methoxy-phenylamine 

Downstream Products

• 1610849-77-8 6-chloro-4-methoxy-9-(2-aminoanilino)acridine hydrochloride 
• 75423-01-7 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(4,5-dimethoxy-2-nitro-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-58-7 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(3-nitro-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-57-6 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(2-nitro-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-63-4 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(4-hydroxy-3-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-62-3 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(4-dimethylamino-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-60-1 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(2-chloro-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-61-2 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(4-chloro-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-59-8 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid [1-(4-hydroxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 75412-41-8 4-Chloro-2-(2-methoxy-phenylamino)-benzoic acid hydrazide 
• 23857-11-6 4-chloro-2-(2-methoxy-anilino)-benzoic acid methyl ester 
• 16095-47-9 7-chloro-1-(2-methoxy-phenyl)-1,2-dihydro-benzo[d][1,3]oxazin-4-one 
• 88914-97-0 6,9-dichloro-4-methoxyacridine 

Relevant articles and documents

A rapid, chromatography-free route to substituted acridine-isoalloxazine conjugates under microwave irradiation

Microwave irradiation was applied to a sequence of condensation reactions from readily available 9-chloroacridines to provide a range of novel acridine-isoalloxazine conjugates. The combination of these two moieties, both of biological interest, was achieved by a chromatography-free route.

Microwave-assisted synthesis of N-phenylanthranilic acids in water

N-Phenylanthranilic acid derivatives were synthesised using the Ullmann condensation of 2-chlorobenzoic acid with aniline derivatives under microwave irradiation in aqueous media. The method offers better yields in shorter reaction times compared to classical heating approaches using water as solvent.

Synthesis and Biological Activity of Some Substituted Diphenylamine-2-carboxylic Acid Derivatives

Twenty-four N-benzylidene-5-chlorodiphenylamine-2-carboxylic acid hydrazides (IV) have been synthesized by condensation of substituted 5-chlorodiphenylamine-2-carboxylic acid hydrazides (III) with different aromatic aldehydes.All the compounds have been s