863418-78-4

Basic information

• Product Name: N-allyl-N-ethyl-4-methyl-benzenesulfonamide
• Synonyms: N-allyl-N-ethyl-4-methyl-benzenesulfonamide
• CAS NO: 863418-78-4
• Molecular Weight: 239.338
• Mol File: 863418-78-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-allyl-N-ethyl-4-methyl-benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-allyl-N-ethyl-4-methyl-benzenesulfonamide(863418-78-4)
• EPA Substance Registry System: N-allyl-N-ethyl-4-methyl-benzenesulfonamide(863418-78-4)

Safety Data

• Hazardous Substances Data: 863418-78-4(Hazardous Substances Data)

Upstream product

• 129748-56-7 N-(2-bromoethyl)-N-(2-propenyl)-4-methylbenzenesulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 1207374-67-1 2-(N-allyl-4-methylphenylsulfonamido)ethyl trifluoromethanesulfonate 
• 80-39-7 N-ethyl-4-methyl-benzenesulfonamide 
• 106-95-6 allyl bromide 

Relevant articles and documents

Method for hydrogenolysis of halides

The invention discloses a method for hydrogenolysis of halides. The invention discloses a preparation method of a compound represented by a formula I. The preparation method comprises the following step: in a polar aprotic solvent, zinc, H2O and a compound represented by a formula II are subjected to a reaction as shown in the specification, wherein X is halogen; Y is -CHRR or R; hydrogenin H2O exists in the form of natural abundance or non-natural abundance. According to the preparation method, halide hydrogenolysis can be simply, conveniently and efficiently achieved through a simple and mild reaction system, and good functional group compatibility and substrate universality are achieved.

Copper-catalyzed trifluoromethylation and cyclization of aromatic-sulfonyl-group-tethered alkenes for the construction of 1,2-benzothiazinane dioxide type compounds

A multi-talented system: An efficient copper-catalyzed tandem trifluoromethylation/annulation of an electron-deficient aromatic ring has been developed. This method provides a powerful and straightforward way to synthesize trifluoromethylated 1,2-benzothiazinane dioxides under mild conditions (see scheme). The mechanism was investigated by a series of kinetic experiments and isotopic labeling studies.

Nickel-catalyzed reductive cyclization of organohalides

A mild and convenient nickel-catalyzed method for free-radical cyclization of organohalides is described. The use of a NiCl2DME/Pybox complex as the catalyst and zinc powder in methanol efficiently promotes the reductive cyclization of various