6435-79-6

Basic information

• Product Name: 2-methyl-1-[(4-methylphenyl)sulfonyl]-pyrrolidine
• Synonyms: 2-methyl-1-[(4-methylphenyl)sulfonyl]-pyrrolidine
• CAS NO: 6435-79-6
• Molecular Weight: 239.338
• Mol File: 6435-79-6.mol
• Article Data: 28

Chemical Properties

• CAS DataBase Reference: 2-methyl-1-[(4-methylphenyl)sulfonyl]-pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-1-[(4-methylphenyl)sulfonyl]-pyrrolidine(6435-79-6)
• EPA Substance Registry System: 2-methyl-1-[(4-methylphenyl)sulfonyl]-pyrrolidine(6435-79-6)

Safety Data

• Hazardous Substances Data: 6435-79-6(Hazardous Substances Data)

Upstream product

• 81097-24-7 N-tosyl-(4-pentenyl)amine 
• 96-47-9 2-methyltetrahydrofuran 
• 70-55-3 toluene-4-sulfonamide 
• 22537-07-1 4-pentenyl-1-amine 
• 104-15-4 toluene-4-sulfonic acid 
• 544-97-8 dimethyl zinc(II) 
• 6435-78-5 N-tosylpyrrolidine 
• 75-16-1 methylmagnesium bromide 
• 110-58-7 n-Pentylamine 
• 145782-19-0 N-(4-pentyn-1-yl)-4-methyl-benzenesulfonamide 
• 626-95-9 1,4-Pentanediol 
• 98-59-9 p-toluenesulfonyl chloride 
• 304460-21-7 rac-4-methyl-N-(pentan-2-yl)benzenesulfonamide 
• 625-30-9 2-pentylamine 

Relevant articles and documents

Intramolecular Hydroalkoxylation/Reduction and Hydroamination/Reduction of Unactivated Alkynes Using a Silane-Iodine Catalytic System

A transition-metal-free silane-iodine catalytic system comprising I 2 and Et 3 SiH promotes intramolecular hydroalkoxylation/reduction and hydroamination/reduction of unactivated alkynes. This system allows the reaction to proceed at room temperature affording 2,4- and 2,5-disubstituted pyrrolidines as well as a 2,3-disubstituted tetrahydrofuran with high diastereoselectivity..

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

Manganese-Catalyzed N-F Bond Activation for Hydroamination and Carboamination of Alkenes

A visible-light-promoted method for generating amidyl radicals from N-fluorosulfonamides via a manganese-catalyzed N-F bond activation strategy is reported. This protocol employs a simple manganese complex, Mn2(CO)10, as the precatalyst and a cheap silane, (MeO)3SiH, as both the hydrogen-atom donor and the F-atom acceptor, enabling intramolecular/intermolecular hydroaminations of alkenes, two-component carboamination of alkenes, and even three-component carboamination of alkenes. A wide range of valuable aliphatic sulfonamides can be readily prepared using these practical reactions.