134452-27-0

Basic information

• Product Name: Benzenesulfonamide, N-[(1S)-1-(2-furanyl)ethyl]-4-methyl-
• CAS NO: 134452-27-0
• Molecular Formula: C13H15NO3S
• Molecular Weight: 265.333
• Mol File: 134452-27-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[(1S)-1-(2-furanyl)ethyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[(1S)-1-(2-furanyl)ethyl]-4-methyl-(134452-27-0)
• EPA Substance Registry System: Benzenesulfonamide, N-[(1S)-1-(2-furanyl)ethyl]-4-methyl-(134452-27-0)

Safety Data

• Hazardous Substances Data: 134452-27-0(Hazardous Substances Data)

Upstream product

• 135822-87-6 (E)-N-(furan-2-ylmethylene)-4-methylbenzenesulfonamide 
• 1240250-19-4 1-(2-furyl)-N-tosylethanimine 
• 1192-62-7 1-(2-furyl)-1-ethanone 
• 916585-21-2 (S,E)-N-(1-furan-2-yl-ethylidene)-p-toluenesulfinamide 
• 134340-62-8 N-(1-furan-2-yl-ethyl)-4-methyl-benzenesulfonamide 
• 917-64-6 methyl magnesium iodide 
• 188447-91-8 (S)-p-toluenesulfinimide 

Downstream Products

• 4816-81-3 p-tosyl-L-alanine 
• 148346-42-3 (2S,6S)-1,6-dihydro-6-hydroxy-2-methyl-N-tosylpyridin-3(2H)-one 
• 148257-03-8 S-methyl O-<(2S,3R,6R)-2-methyl-6-propyl-N-tosylpiperidin-3-yl> dithiocarbonate 
• 148346-41-2 (2S,6S)-6-ethoxy-1,6-dihydro-2-methyl-N-tosylpyridin-3(2H)-one 
• 150222-14-3 (2S,3R,6S)-6-allyl-2-methyl-N-tosylpiperidin-3-ol 
• 148256-99-9 (2S,3R,6S)-6-ethoxy-2-methyl-N-tosylpiperidin-3-ol 
• 148257-02-7 (2S,3R,6R)-2-methyl-6-propyl-N-tosylpiperidin-3-ol 

Relevant articles and documents

Highly enantioselective Rh-catalyzed transfer hydrogenation of N-sulfonyl ketimines

Several imine species comprising N-sulfinyl and N-sulfonyl ketimine, oxime, and enamine derivatives were subjected to asymmetric transfer hydrogenation in an azeotropic mixture of formic acid/triethylamine. Among them, the Rh-catalyzed transfer hydrogenat

An efficient preparation of optically active α-furfuryl amide by kinetic resolution using the modified Sharpless asymmetric epoxidation reagents

Kinetic resolution of α-furfuryl amide was first carried out by using the modified Sharpless asymmetric epoxidation reagent to give the slow-reacting enantiomers, (S)-1(a-h) and (R)-1(b,f) in high enantioselectivity (90-100% e.e) and high chemical yield (