23289-99-8

Basic information

• Product Name: Benzeneethanesulfonyl chloride, b-oxo-
• CAS NO: 23289-99-8
• Molecular Formula: C8H7ClO3S
• Molecular Weight: 218.661
• Mol File: 23289-99-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzeneethanesulfonyl chloride, b-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanesulfonyl chloride, b-oxo-(23289-99-8)
• EPA Substance Registry System: Benzeneethanesulfonyl chloride, b-oxo-(23289-99-8)

Safety Data

• Hazardous Substances Data: 23289-99-8(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 4496-92-8 benzoylmethanesulfonic acid 

Downstream Products

• 60419-85-4 5-methyl-4,7-diphenyl-1,7-dihydro-pyrazolo[3,4-c][1,2]thiazine 2,2-dioxide 
• 32116-85-1 3-cyclohexyl-2,6-diphenyl-2,3-dihydro-[1,4,3]oxathiazine 4,4-dioxide 
• 32116-84-0 3-benzyl-2,6-diphenyl-2,3-dihydro-[1,4,3]oxathiazine 4,4-dioxide 
• 32116-89-5 (2-benzyl-1,1-dioxo-3-phenyl-1λ⁶-[1,2]thiazetidin-4-yl)-phenyl-methanone 
• 35810-48-1 1,1'-diphenyl-2,2'-(2-morpholin-4-yl-cyclohex-1-ene-1,3-disulfonyl)-bis-ethanone 
• 32116-96-4 2,6,2',6'-tetraphenyl-2,3,2',3'-tetrahydro-3,3'-ethane-1,2-diyl-bis-[1,4,3]oxathiazine 4,4,4',4'-tetraoxide 
• 32116-83-9 2,6-diphenyl-3-propyl-2,3-dihydro-[1,4,3]oxathiazine 4,4-dioxide 
• 32116-90-8 (1,1-dioxo-3-phenyl-2-propyl-1λ⁶-[1,2]thiazetidin-4-yl)-phenyl-methanone 
• 66004-07-7 [1-(4-chloro-phenyl)-2,2-dioxo-(3ar)-1,2,3,3a-tetrahydro-2λ⁶-cyclohepta[c]isothiazol-3c-yl]-phenyl-methanone 
• 66004-06-6 [1-(4-methoxy-phenyl)-2,2-dioxo-(3ar)-1,2,3,3a-tetrahydro-2λ⁶-cyclohepta[c]isothiazol-3c-yl]-phenyl-methanone 
• 58044-83-0 N-Phenacylsulfonyl-n-butylamin 
• 7117-22-8 2-oxo-N,2-diphenylethane-1-sulfonamide 
• 16261-68-0 4-phenyl-3H-benzo[f][1,2,5]oxathiazepine 2,2-dioxide 
• 59043-88-8 (2,2-dioxo-4t-phenyl-2,3,4,5-tetrahydro-2λ⁶-benzo[f][1,2,5]oxathiazepin-3r-yl)-phenyl-methanone 

Relevant articles and documents

Highly enantioselective synthesis of β-hydroxysulfonamides by asymmetric transfer hydrogenation

A series of optically active β-hydroxy sulfonamides were synthesized for the first time by asymmetric transfer hydrogenation of the corresponding β-ketosulfonamides using the Ru-TsDPEN-HCOOH-Et3N catalytic system, in excellent yields (up to 95%