172606-16-5

Basic information

• Product Name: Benzenesulfonamide, N-[2-(2-cyclohexen-1-yl)ethyl]-4-methyl-
• CAS NO: 172606-16-5
• Molecular Formula: C15H21NO2S
• Molecular Weight: 279.403
• Mol File: 172606-16-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[2-(2-cyclohexen-1-yl)ethyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[2-(2-cyclohexen-1-yl)ethyl]-4-methyl-(172606-16-5)
• EPA Substance Registry System: Benzenesulfonamide, N-[2-(2-cyclohexen-1-yl)ethyl]-4-methyl-(172606-16-5)

Safety Data

• Hazardous Substances Data: 172606-16-5(Hazardous Substances Data)

Upstream product

• 53916-68-0 2-(cyclohex-2-enyl)ethylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 672903-58-1 2-(2-cyclohexenyl)ethyl methanesulfonate 
• 18522-92-4 sodium p-toluenesulfonamide 
• 112052-21-8 methyl 2-(cyclohex-2-en-1-yl)acetate 
• 16452-34-9 2-(cyclohex-2-enyl)ethanol 
• 34939-28-1 dimethyl 2-(cyclohex-2-en-1-yl)malonate 
• 76644-52-5 rac-3-acetoxycyclohexene 

Relevant articles and documents

Aza-heterocycles via copper-catalyzed, remote C–H desaturation of amines

A majority of medicines contain a nitrogen atom within a five- or six-membered ring. To rapidly access both such aza-heterocycles, we sought to develop a remote C–H desaturation of amines. Inspired by the Hofmann-L?ffler-Freytag (HLF) synthesis of five-me

Palladium(II)-catalyzed cyclization using molecular oxygen as reoxidant

A palladium(II)-catalyzed intramolecular allylic oxidations using, nitrogen and oxygen nucleophiles and molecular oxygen as reoxidant has been developed.