24865-83-6

Basic information

• Product Name: Benzenesulfonamide, 4-methyl-N-(1-phenylethylidene)-
• CAS NO: 24865-83-6
• Molecular Formula: C15H15NO2S
• Molecular Weight: 273.356
• Mol File: 24865-83-6.mol
• Article Data: 36

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-(1-phenylethylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-(1-phenylethylidene)-(24865-83-6)
• EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-(1-phenylethylidene)-(24865-83-6)

Safety Data

• Hazardous Substances Data: 24865-83-6(Hazardous Substances Data)

Upstream product

• 70-55-3 toluene-4-sulfonamide 
• 98-86-2 acetophenone 
• 6873-55-8 p-tolylsulfinyl amide 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 81801-27-6 (+/-)-(S,E)-N-(1-Phenylethylidene)toluene-p-sulfinamide 
• 672-78-6 methyl p-toluene sulfinate 
• 177468-94-9 N-(α-methyl-benzylidene)-p-toluenesulfinamide 
• 100-42-5 styrene 
• 51608-60-7 phenyl N-tosyl imine 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 10341-75-0 (E)-1-phenylethanone oxime 
• 98-59-9 p-toluenesulfonyl chloride 
• 4809-56-7 N-(1-phenylethyl)-p-toluenesulfonamide 
• 24395-14-0 N-(p-tolylsulfonyl)-2-phenylaziridine 

Downstream Products

• 72984-27-1 4-Methyl-N-((R)-1-phenyl-ethyl)-benzenesulfonamide 
• 1283154-36-8 N-(1-(dimethyl(phenyl)silyl)-1-phenylethyl)-4-methylbenzenesulfonamide 
• 36283-44-0 N-acetyl-1-phenylethylamine 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 66558-04-1 N-[(1S)-1-phenylethan-1-yl]-4-methylbenzenesulfonamide 
• 13398-26-0 (S)-2-methyl-2-phenylglycine 

Relevant articles and documents

A new preparation of cis-N-sulfonylaziridines from N-sulfonylaldimines using trimethylsilyldiazomethane

Trimethylsilyldiazomethane smoothly reacts with N-sulfonylaldimines to give 2-substituted N-sulfonyl-3-trimethylsilylaziridines in good yields with high cis selectivity. (C) 2000 Elsevier Science Ltd.

Methyltrioxorhenium/urea hydrogen peroxide catalyzed oxidation of N-sulfinyl imines: A mild and highly efficient access to N-sulfonyl aldimines, ketimines and α-ketiminoesters

A mild and highly efficient access to N-sulfonyl imines through the oxidation of corresponding N-tert-butylsulfinyl imines and N-p-tosyl-sulfinyl imines with UHP in the presence of catalytic amount MTO was developed. Under mild reaction conditions, this h

Catalyst-controlled regiodivergent ring-opening C(sp3)-Si bond-forming reactions of 2-arylaziridines with silylborane enabled by synergistic palladium/copper dual catalysis

A catalyst-controlled regiodivergent and stereospecific ring-opening C(sp3)-Si cross-coupling of 2-arylaziridines with silylborane enabled by synergistic Pd/Cu dual catalysis has been developed. Just by selecting a suitable combination of catalysts, the regioselectivity of the coupling is completely switched to efficiently provide two regioisomers of β-silylamines (i.e., β-silyl-α-phenethylamines and β-silyl-β-phenethylamines) in good to high yields. Furthermore, a slight modification of the reaction conditions caused a drastic change in reaction pathways, leading to a tandem reaction to produce another regioisomer of silylamine (i.e., α-silyl-β-phenethylamines) in an efficient and selective manner.