107642-74-0

Basic information

• Product Name: 2,4-dimethyl-6-(4-methylphenylsulfonamido)benzoic acid
• CAS NO: 107642-74-0
• Molecular Weight: 319.381
• Mol File: 107642-74-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,4-dimethyl-6-(4-methylphenylsulfonamido)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dimethyl-6-(4-methylphenylsulfonamido)benzoic acid(107642-74-0)
• EPA Substance Registry System: 2,4-dimethyl-6-(4-methylphenylsulfonamido)benzoic acid(107642-74-0)

Safety Data

• Hazardous Substances Data: 107642-74-0(Hazardous Substances Data)

Upstream product

• 90321-33-8 2-amino-4,6-dimethyl-benzoic acid 
• 49820-06-6 4,6-dimethyl-1H-indole-2,3-dione 
• 1570134-98-3 N-(2-(4,5-dihydrooxazol-2-yl)phenyl)-2,4-dimethyl-6-(4-methylphenylsulfonamido)benzamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 941-55-9 4-toluenesulfonyl azide 
• 611-01-8 2,4-dimethyl-benzoic acid 

Downstream Products

• 107642-75-1 4-methoxy-3,4',5,6'-tetramethyl-2'-(4-toluenesulphonamino)diphenyl ketone 
• 107642-76-2 2'-amino-4-methoxy-3,4',5,6'-tetramethyldiphenyl ketone 
• 114097-28-8 N-(3,5-dimethylphenyl)-4-methyl-benzenesulfonamide 

Relevant articles and documents

Method for Preparing Derivatives of Anthranilic acid and Anti-inflammatory Use Thereof

The present invention relates to a production method of anthranilic acid derivatives which reacts benzoic acid derivatives and phenylsulfonyl azide derivatives under the presence of a [IrCp*Cl_2]_2 catalyst; and relates to an anti-inflammatory use of the

Cu(II)-mediated C-H amidation and amination of arenes: Exceptional compatibility with heterocycles

A Cu(OAc)2-mediated C-H amidation and amination of arenes and heteroarenes has been developed using a readily removable directing group. A wide range of sulfonamides, amides, and anilines function as amine donors in this reaction. Heterocycles present in both reactants are tolerated, making this a broadly applicable method for the synthesis of a family of inhibitors including 2-benzamidobenzoic acids and N-phenylaminobenzoates.