861527-11-9

Basic information

• Product Name: 2-(2-(phenylsulfonamido)benzamido)benzoic acid
• Synonyms: 2-(2-(phenylsulfonamido)benzamido)benzoic acid
• CAS NO: 861527-11-9
• Molecular Weight: 396.423
• Mol File: 861527-11-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2-(phenylsulfonamido)benzamido)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-(phenylsulfonamido)benzamido)benzoic acid(861527-11-9)
• EPA Substance Registry System: 2-(2-(phenylsulfonamido)benzamido)benzoic acid(861527-11-9)

Safety Data

• Hazardous Substances Data: 861527-11-9(Hazardous Substances Data)

Upstream product

• 68506-37-6 2-(2-nitrobenzamido)benzoic acid 
• 10128-51-5 N-(2-(4-oxo-4H-benzo[d][1,3]oxazin-2-yl)phenyl)benzenesulfonamide 
• 938-10-3 phenylsulfonyl azide 
• 1022-46-4 2-phenyl-4H-3,1-benzoxazin-4-one 
• 610-14-0 2-nitrobenzyl chloride 
• 37960-65-9 potassium anthranilate 
• 612-34-0 N-anthraniloyl-anthranilic acid 
• 98-09-9 benzenesulfonyl chloride 
• 714205-51-3 N-(N-benzenesulfonyl-anthraniloyl)-anthranilic acid ethyl ester 

Downstream Products

• 10128-51-5 N-(2-(4-oxo-4H-benzo[d][1,3]oxazin-2-yl)phenyl)benzenesulfonamide 

Relevant articles and documents

Ruthenium catalyzed chemo and site-selective C-H amidation of oxobenzoxazine derivatives with sulfonyl azides

An efficient, novel and general protocol towards the synthesis of highly functionalized ortho-amido oxobenzoxazine frameworks via ruthenium catalyzed intermolecular C-H amidation using sulfonyl azides as amidation components has been successfully developed for the first time. The salient features of this strategy are high chemo and site-selectivity, a wide range of substrate scope with excellent yields and good functional group tolerance.