389079-71-4

Basic information

• Product Name: N-(2-(cyclohex-1-en-1-yl)ethyl)-4-methylbenzenesulfonamide
• Synonyms: N-(2-(cyclohex-1-en-1-yl)ethyl)-4-methylbenzenesulfonamide
• CAS NO: 389079-71-4
• Molecular Weight: 279.403
• Mol File: 389079-71-4.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: N-(2-(cyclohex-1-en-1-yl)ethyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(cyclohex-1-en-1-yl)ethyl)-4-methylbenzenesulfonamide(389079-71-4)
• EPA Substance Registry System: N-(2-(cyclohex-1-en-1-yl)ethyl)-4-methylbenzenesulfonamide(389079-71-4)

Safety Data

• Hazardous Substances Data: 389079-71-4(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 3399-73-3 2-(1-cyclohexenyl)ethylamine 
• 624-31-7 4-tolyl iodide 
• 3197-68-0 2-(1-Cyclohexenyl)ethanol 
• 18294-87-6 1-cyclohexenylacetic acid 

Downstream Products

• 129748-75-0 (3aR*,7aR*)-1-(toluene-4-sulfonyl)octahydroindole 

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

Iridium-Catalyzed Cycloisomerization of N-Tethered 1,7-Enynes: Construction of an Azabicyclo[5.1.0]octene System

An efficient method for the synthesis of azabicyclo[5.1.0]octenes through cycloisomerization of nitrogen-tethered 1,7-enynes catalyzed by [IrCp*Cl2]2 was developed. With appropriately designed substrates, this method could be easily employed to generate complex fused ring systems such as [6-6-3-7], [5-6-3-7], [7-6-3-7], and [8-6-3-7] ring systems, which enriches the diversity of the cyclopropane-fused polycycle library, and has potential applications in SAR studies of pharmaceutically interesting compounds and total synthesis of natural products.

DIRECT ANTI-MARKOVNIKOV ADDITION OF ACIDS TO ALKENES

A method of making an anti-Markovnikov addition product, comprises reacting an acid with an alkene or alkyne in a dual catalyst reaction system to the exclusion of oxygen to produce said anti-Markovnikov addition product; the dual catalyst reaction system comprising a single electron oxidation catalyst in combination with a hydrogen atom donor catalyst. Dual catalyst composition useful for carrying out such methods are also described.