94631-72-8

Basic information

• Product Name: Benzoic acid, 2-[(3-chloro-4-methoxyphenyl)amino]-
• CAS NO: 94631-72-8
• Molecular Formula: C14H12ClNO3
• Molecular Weight: 277.707
• Mol File: 94631-72-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-[(3-chloro-4-methoxyphenyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-[(3-chloro-4-methoxyphenyl)amino]-(94631-72-8)
• EPA Substance Registry System: Benzoic acid, 2-[(3-chloro-4-methoxyphenyl)amino]-(94631-72-8)

Safety Data

• Hazardous Substances Data: 94631-72-8(Hazardous Substances Data)

Upstream product

• 5345-54-0 3-chloro-4-methoxyaniline 
• 118-91-2 ortho-chlorobenzoic acid 

Downstream Products

• 1368178-09-9 1-[2-(3-chloro-4-methoxyphenylamino)phenyl]ethanone 
• 98156-60-6 N-(3-chloro-4-methoxy-phenyl)-anthranilic acid ethyl ester 
• 731817-37-1 N-(3-chloro-4-methoxy-phenyl)-anthraniloyl chloride 

Relevant articles and documents

Substituted aminobenzamides and their use as agents which inhibit lipoxygenase activity

Novel 2-(hydroxyphenylamino)benzamides and oxidation products thereof, useful as inhibitors of lipoxygenase, are of the formulas STR1 wherein R is hydrogen, lower-alkyl, halo or lower-alkoxy; R' is hydrogen or lower-alkyl; R" is hydrogen, lower-alkyl or halo; and N=Z is amino or substituted amino. The compounds of Formula I are prepared by de-etherification of the corresponding alkyl or benzyl ethers; and the compounds of Formula II are prepared by oxidation of the compounds of Formula I where R' is hydrogen and OH is in the 4-position.

Substituted aminophenylalkyl ketones, their preparation and use

Novel lower-alkyl 2-(hydroxyphenylamino)phenyl ketones, useful as inhibitors of lipoxygenase activity, are of the formula STR1 wherein R is hydrogen, lower-alkyl, lower-alkoxy or halo; R' is hydrogen or lower-alkyl; R" is hydrogen, lower-alkyl or halo; and Alk is lower-alkyl. The compounds are prepared by de-etherification of the corresponding alkyl or benzyl ethers which are in turn prepared by reacting a 2-(alkoxy- or benzyloxyphenylamino)benzoic acid with an alkyllithium.