97399-11-6

Basic information

• Product Name: Benzenesulfonamide, N-2-cyclohepten-1-yl-4-methyl-
• CAS NO: 97399-11-6
• Molecular Formula: C14H19NO2S
• Molecular Weight: 265.376
• Mol File: 97399-11-6.mol

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-2-cyclohepten-1-yl-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-2-cyclohepten-1-yl-4-methyl-(97399-11-6)
• EPA Substance Registry System: Benzenesulfonamide, N-2-cyclohepten-1-yl-4-methyl-(97399-11-6)

Safety Data

• Hazardous Substances Data: 97399-11-6(Hazardous Substances Data)

Upstream product

• 826-13-1 2-cycloheptenyl acetate 
• 18522-92-4 sodium p-toluenesulfonamide 
• 628-92-2 Cycloheptene 
• 55962-05-5 4-methyl-N-[(E)-phenyl-λ³-iodanylidene]benzenesulfonamide 

Downstream Products

• 339541-03-6 2-hex-5-enyl-1-(toluene-4-sulfonyl)-4-vinyl-2,5-dihydro-1H-pyrrole 
• 339540-96-4 N-(cyclohept-2-en-1-yl)-4-methyl-N-(prop-2-yn-1-yl)benzenesulfonamide 

Relevant articles and documents

Mn(salen)-catalyzed enantioselective C-H amination

A chiral 3,3′,5,5′-tetrabromosubstituted (salen)manganese(III) complex was found to be an efficient catalyst for asymmetric C-H amination (up to 89% ee). In the reaction of cycloalkenes, allylic amination occurred in preference to aziridination.

SYNTHESIS OF PROTECTED ALLYLAMINES VIA PALLADIUM-CATALYZED AMIDE ADDITION TO ALLYLIC SUBSTRATES

Palladium-catalyzed reaction of allylic substrates with sodium p-toluenesulfonamide leads to the N-allylic-p-toluenesulfonamides.The reaction takes place with retention of configuration at the allylic carbon.