134340-63-9

Basic information

• Product Name: Benzenesulfonamide, N-[1-(2-furanyl)propyl]-4-methyl-
• CAS NO: 134340-63-9
• Molecular Formula: C14H17NO3S
• Molecular Weight: 279.36
• Mol File: 134340-63-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[1-(2-furanyl)propyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[1-(2-furanyl)propyl]-4-methyl-(134340-63-9)
• EPA Substance Registry System: Benzenesulfonamide, N-[1-(2-furanyl)propyl]-4-methyl-(134340-63-9)

Safety Data

• Hazardous Substances Data: 134340-63-9(Hazardous Substances Data)

Upstream product

• 135822-87-6 (E)-N-(furan-2-ylmethylene)-4-methylbenzenesulfonamide 
• 811-49-4 ethyllithium 
• 110-00-9 furan 
• 123-38-6 propionaldehyde 
• 4104-47-6 N-sulfinyl-p-toluenesulfonamide 
• 98-01-1 furfural 
• 70-55-3 toluene-4-sulfonamide 
• 13707-47-6 2-furaldehyde tosylimine 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 134340-69-5 C₁₄H₁₇NO₄S 
• 1188297-03-1 N-(1-furan-2-yl-propyl)-N-[3-(4-methoxyphenoxy)prop-2-yn-1-yl]-4-methylbenzenesulfonamide 
• 134452-33-8 N-[(1R)-1-(furan-2-yl)propan-1-yl]-4-methylbenzenesulfonamide 
• 134452-28-1 N-[(1S)-1-(furan-2-yl)propan-1-yl]-4-methylbenzenesulfonamide 
• 134340-69-5 (S)-2-Ethyl-6-hydroxy-1-(toluene-4-sulfonyl)-1,6-dihydro-2H-pyridin-3-one 
• 134340-69-5 (R)-2-Ethyl-6-hydroxy-1-(toluene-4-sulfonyl)-1,6-dihydro-2H-pyridin-3-one 
• 944063-41-6 C₁₅H₁₉NO₄S 

Relevant articles and documents

Chiral binaphthylthiophosphoramide - Cu(I)-catalyzed asymmetric addition of diethylzinc to N-sulfonylimines

In the presence of a catalytic amount of chiral binaphthylthiophosphoramide L2 (6 mol %) and Cu(I) (3 mol %), the asymmetric addition of diethylzinc to N-sulfonylimines could be achieved in good yields with moderate to high ee (63-93% ee) at 0 °C in tolue

Synthesis of 2-aza-1-cyano-4-hydroxyanthraquinones

Phthalide annulation of 2-alkylpyridin-3-ones results in the formation of the unexpected 2-aza-1-cyano-4-hydroxy-anthraquinones, the cyano moiety originating from the 3-cyanophthalide. These compounds hold great potential against Epstein-Barr Virus Early

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 (