924107-85-7

Basic information

• Product Name: 2-bromo-N-(2-methoxyphenyl)benzenesulfonamide
• Synonyms: 2-bromo-N-(2-methoxyphenyl)benzenesulfonamide
• CAS NO: 924107-85-7
• Molecular Weight: 342.213
• Mol File: 924107-85-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-bromo-N-(2-methoxyphenyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-N-(2-methoxyphenyl)benzenesulfonamide(924107-85-7)
• EPA Substance Registry System: 2-bromo-N-(2-methoxyphenyl)benzenesulfonamide(924107-85-7)

Safety Data

• Hazardous Substances Data: 924107-85-7(Hazardous Substances Data)

Upstream product

• 2905-25-1 o-bromobenzenesulfonyl chloride 
• 90-04-0 2-methoxy-phenylamine 

Downstream Products

• 1453106-47-2 2-(2-methoxyphenyl)-3-methylene-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide 
• 1453106-54-1 2-(2-methoxyphenyl)-3'-phenyl-2H,4’H-spiro[benzo[d]isothiazole-3,5'-isoxazole] 1,1-dioxide 
• 1453106-40-5 N-(2-methoxyphenyl)-2-((trimethylsilyl)ethynyl)benzenesulfonamide 
• 1582316-68-4 2-bromo-N-(but-3-en-1-yl)-N-(2-methoxyphenyl)benzenesulfonamide 
• 1582316-82-2 2-(2-methoxyphenyl)-3'-phenyl-3,4-dihydro-2H,4'H-spiro[benzo[f][1,2]thiazepine-5,5'-isoxazole] 1,1-dioxide 
• 1582316-75-3 2-(2-methoxyphenyl)-5-methylene-2,3,4,5-tetrahydrobenzo[f][1,2]thiazepine 1,1-dioxide 
• 1391741-60-8 2-(4-methoxyphenoxy)-N-(2-methoxyphenyl)benzenesulfonamide 

Relevant articles and documents

Benzonitrile oxide cycloadditions with exocyclic methylene benzothiazepine dioxides

N-substituted 5-methylene-2,3,4,5-tetrahydrobenzo[f][1,2]thiazepine 1,1-dioxides underwent 1,3-dipolar cycloaddition with benzonitrile oxide, generated in situ, to give isoxazoline spiro adducts. The cycloadditions were completely regioselective to give the hitherto unreported 3,4-dihydro-2H, 4′ H-spiro[benzo[f][1,2]thiazepine-5, 5′-isoxazole] 1,1-dioxide cycloadduct. Where the N-substituent on the sulfonamide cycloaddition precursor was a 2-substituted arene, the resulting atropisomerism along the N-aryl bond led to facial selectivity in the cycloaddition reaction, with greater than 90% diastereoselectivity. CSIRO 2014.