115125-88-7

Basic information

• Product Name: (E)-N,N-dimethyl-4-tosylbut-2-enylamine
• Synonyms: (E)-N,N-dimethyl-4-tosylbut-2-enylamine
• CAS NO: 115125-88-7
• Molecular Weight: 253.365
• Mol File: 115125-88-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-N,N-dimethyl-4-tosylbut-2-enylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N,N-dimethyl-4-tosylbut-2-enylamine(115125-88-7)
• EPA Substance Registry System: (E)-N,N-dimethyl-4-tosylbut-2-enylamine(115125-88-7)

Safety Data

• Hazardous Substances Data: 115125-88-7(Hazardous Substances Data)

Upstream product

• 85615-58-3 1-(p-methylbenzenesulfonyl)-1,3-butadiene 
• 124-40-3 dimethyl amine 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 115147-52-9 (E)-1-iodo-4-tosyl-2-butene 

Downstream Products

• 188430-53-7 (E)-4-methyl-1-dimethylamino-4-tosyl-2-pentene 

Relevant articles and documents

"Syn effect" in nucleophilic addition of amines to 1,3-dienyl sulfone and ethyl (E)-2,4-pentadienoate

The stereochemistry of nucleophilic addition of amines to (E)-l-tosyl-l,3-butadiene was investigated. The Z/E ratios of the resulting allylic sulfones varied with amines, solvents, temperature, and concentration. When diethylamine was reacted in low conce

Synthesis of Allyl and Dienyl Sulphones via Iodosulphonylation of Conjugated Dienes

The iodosulphonylation of conjugated dienes with sodium or mercury(II) toluene-p-sulphinate and iodine yields δ-iodoalkenyl sulphones stereoselectively.These compounds undergo stereospecific dehydrohalogenation to afford dienyl sulphones and nucleophilic