1022287-61-1

Basic information

• Product Name: N-(1,1-dioxo-1H-1λ⁶-benzo[b]thiophen-6-yl)-4-methylbenzenesulfonamide
• Synonyms: N-(1,1-dioxo-1H-1λ⁶-benzo[b]thiophen-6-yl)-4-methylbenzenesulfonamide
• CAS NO: 1022287-61-1
• Molecular Weight: 335.405
• Mol File: 1022287-61-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(1,1-dioxo-1H-1λ⁶-benzo[b]thiophen-6-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1,1-dioxo-1H-1λ⁶-benzo[b]thiophen-6-yl)-4-methylbenzenesulfonamide(1022287-61-1)
• EPA Substance Registry System: N-(1,1-dioxo-1H-1λ⁶-benzo[b]thiophen-6-yl)-4-methylbenzenesulfonamide(1022287-61-1)

Safety Data

• Hazardous Substances Data: 1022287-61-1(Hazardous Substances Data)

Upstream product

• 20503-40-6 1,1-dioxo-1H-1λ6-benzo[b]thiophen-6-ylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 17347-32-9 6-bromobenzothiophene 
• 937610-19-0 N-(benzo[b]thiophen-6-yl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Enantioselective hydroarylation or hydroalkenylation of benzo[b]thiophene 1,1-dioxides with organoboranes

An efficient protocol for the asymmetric hydroarylation and hydroalkenylation of benzo[b]thiophene 1,1-dioxides with organoboranes has been developed. The combination of a rhodium(I) precatalyst and a chiral diene ligand constitutes the catalytic system, which enables the facile synthesis of 2,3-dihydrobenzo[b]thiophene 1,1-dioxides in good yields with high enantioselectivities. The merging of this asymmetric hydroarylation with the downstream alkylations delivers 2,3-dihydrobenzo[b]thiophene 1,1-dioxides that contain two continuous quaternary stereocenters with high enantioselectivities in a diastereodivergent manner.