260975-29-9

Basic information

• Product Name: (E)-N-cyclohexylmethylene-4-toluenesulfonamide
• Synonyms: (E)-N-cyclohexylmethylene-4-toluenesulfonamide
• CAS NO: 260975-29-9
• Molecular Weight: 265.376
• Mol File: 260975-29-9.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: (E)-N-cyclohexylmethylene-4-toluenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-cyclohexylmethylene-4-toluenesulfonamide(260975-29-9)
• EPA Substance Registry System: (E)-N-cyclohexylmethylene-4-toluenesulfonamide(260975-29-9)

Safety Data

• Hazardous Substances Data: 260975-29-9(Hazardous Substances Data)

Upstream product

• 86328-85-0 N-(cyclohexylmethyl)-4-methylbenzenesulfonamide 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 70-55-3 toluene-4-sulfonamide 
• 1323310-70-8 N-(cyclohexyl(phenylsulfonyl)methyl)-p-toluenesulfonamide 
• 2043-61-0 cyclohexanecarbaldehyde 

Downstream Products

• 1369862-26-9 C₁₄H₁₉NO₃S 
• 1198790-83-8 N-(1-cyclohexyl-3-oxo-3-phenylpropyl)-4-methyl benzenesulfonamide 
• 1112116-79-6 (S)-N-[(cyclohexyl)phenylmethyl]-4-methylbenzenesulfonamide 
• 1611478-33-1 (R)-N-{[dimethyl(phenyl)silyl](cyclohexyl)methyl}-4-toluenesulfonamide 
• 1447965-17-4 2-(2-cyclohexyl-3-tosyloxazolidin-4-yl)-1-phenylethanone 
• 1447965-18-5 2-(2-cyclohexyl-3-tosyloxazolidin-4-yl)-1-phenylethanone 

Relevant articles and documents

Ni(0)-Catalyzed Three-Component Coupling Reaction of Tetrafluoroethylene and N-Sulfonyl-Substituted Imines with Silanes via Aza-Nickelacycles

A nickel-catalyzed three-component coupling reaction of tetrafluoroethylene (TFE) and N-sulfonyl-substituted imines with silanes that furnishes a variety of fluorine-containing amines is disclosed. Stoichiometric experiments revealed that the aza-nickelac

Direct Mannich-Type Reactions Promoted by Frustrated Lewis Acid/Br?nsted Base Catalysts

Direct Mannich-type reactions that afford both α- and β-amino esters by the reaction of a broad range of carbonyl compounds and aldimines are disclosed. The transformation is promoted by a sterically frustrated Lewis acid/Br?nsted base pair, which is prop

Diastereoselective Johnson-Corey-Chaykovsky trifluoroethylidenation

(2,2,2-Trifluoroethyl)diphenylsulfonium triflate was found to be an efficient ylide reagent for the Johnson-Corey-Chaykovsky reaction to afford trifluoromethyl epoxides, cyclopropanes and aziridines. Interestingly, excellent but different diastereoselectivity was observed for these transformations. Both trifluoromethyl epoxides and cyclopropanes were obtained with trans-selectivity, whereas aziridines were obtained with cis-selectivity.