108223-53-6

Basic information

• Product Name: Benzenesulfonamide, N-2-cyclohexen-1-yl- (9CI)
• Synonyms: Benzenesulfonamide, N-2-cyclohexen-1-yl- (9CI)
• CAS NO: 108223-53-6
• Molecular Formula: C₁₂H₁₅NO₂S
• Molecular Weight: 237.318
• Product Categories: SULFONAMIDE
• Mol File: 108223-53-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzenesulfonamide, N-2-cyclohexen-1-yl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-2-cyclohexen-1-yl- (9CI)(108223-53-6)
• EPA Substance Registry System: Benzenesulfonamide, N-2-cyclohexen-1-yl- (9CI)(108223-53-6)

Safety Data

• Hazardous Substances Data: 108223-53-6(Hazardous Substances Data)

Upstream product

• 98-10-2 benzenesulfonamide 
• 110-83-8 cyclohexene 
• 286-20-4 cyclohexane-1,2-epoxide 
• 71559-13-2 2-azido cyclohexanol 
• 286-18-0 7-azabicyclo[4.1.0]heptane 
• 127-52-6 chloramine-B 
• 1165952-91-9 cyclohexa-1,3-diene 
• 81097-47-4 N-benzenesulfonyl-7-azabicyclo<4.1.0>heptane 
• 108223-43-4 bis(N-sodiophenylsulfonylamino)selenium dichloride 

Relevant articles and documents

Bismuth-catalyzed intermolecular hydroamination of 1,3-dienes with carbamates, sulfonamides, and carboxamides

A Bi(OTf)3/Cu(CH3CN)4PF6 system efficiently promoted intermolecular 1:1 hydroamination of 1,3-dienes with various carbamates, sulfonamides, and carboxamides to afford allylic amines in good yield (up to 96%). Re

Copper-catalyzed amidation of allylic and benzylic C-H bonds

(Chemical Equation Presented) A copper-catalyzed amidation of allylic and benzylic C-H bonds with both primary and secondary sulfonamides is described. The reaction is applicable to the coupling of a diverse set of hydrocarbon species with aryl, heteroaryl, and alkyl sulfonamides and is tolerant of a variety of functional groups. Mechanistic insight has been gained through the isolation of a benzylic acetate intermediate, which was demonstrated to undergo facile conversion to the substituted sulfonamide product under copper catalysis.

Heteropoly acids: a green and efficient heterogeneous Br?nsted acidic catalyst for the intermolecular hydroamination of olefins

Intermolecular hydroamination of non-activated olefins with amides and benzyl carbamate proceeds efficiently in the presence of environmentally benign silicotungstic acid (HSiW) catalyst under mild conditions in air to afford addition products in good to excellent yields.

Base-promoted elaboration of aziridines

The base-promoted isomerization of aziridines to allyl amines is still an almost unknown reaction. However, the use of superbasic reagents has shown to be able to promote a regio- and stereoselective conversion of monocyclic and bicyclic sulfonyl aziridin

DERIVATIVES OF SELENIUM DIIMIDE

The reaction of selenium with N-sodio-N-chlorobenzenesulfonamide and N-sodio-N-chloro-p-toluenesulfonamide leads to the formation of derivatives of orthoselenious acid, i.e., bis(N-sodioarylsulfonylamino)selenium dichlorides.