796966-23-9

Basic information

• Product Name: (R)-N-((4-chlorophenyl)(4-methoxyphenyl)methyl)-4-methylbenzenesulfonamide
• Synonyms: (R)-N-((4-chlorophenyl)(4-methoxyphenyl)methyl)-4-methylbenzenesulfonamide
• CAS NO: 796966-23-9
• Molecular Weight: 401.914
• Mol File: 796966-23-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (R)-N-((4-chlorophenyl)(4-methoxyphenyl)methyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-N-((4-chlorophenyl)(4-methoxyphenyl)methyl)-4-methylbenzenesulfonamide(796966-23-9)
• EPA Substance Registry System: (R)-N-((4-chlorophenyl)(4-methoxyphenyl)methyl)-4-methylbenzenesulfonamide(796966-23-9)

Safety Data

• Hazardous Substances Data: 796966-23-9(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 70-55-3 toluene-4-sulfonamide 
• 7294-51-1 2,4,6-tris(4-methoxyphenyl)boroxine 
• 357417-22-2 N-(4-chlorobenzylidene)-4-methylbenzenesulfonamide 
• 3157-65-1 N-(p-chlorobenzylidene)-p-toluenesulfonamide 
• 14674-38-5 N-(4-methoxybenzylidene)-p-toluenesulfonamide 
• 1679-18-1 4-Chlorophenylboronic acid 
• 5720-07-0 4-methoxyphenylboronic acid 
• 14674-38-5 (E)-N-(4-methoxybenzylidene)-4-methylbenzenesulfonamide 
• 7519-91-7 tris(4-chlorophenyl)boroxine 

Relevant articles and documents

Synthesis of Chiral Cleft C,N-Palladium and Iridium Complexes from 2,3:6,7-Dibenzobicyclo[3.3.1]nona-2,6-diene-4,8-dione and Their Synthetic Applications

A transition-metal-mediated functionalization of 2,3:6,7-dibenzobicyclo[3.3.1]nona-2,6-diene-4,8-dione is reported. By the use of the corresponding imine, iridium or palladium complexes were prepared, and they were well characterized by NMR and single-cry

Exogenous-Base-Free Palladacycle-Catalyzed Highly Enantioselective Arylation of Imines with Arylboroxines

Enantiomerically pure benzylic amines are important for the development of new drugs. A readily accessible planar-chiral ferrocene-derived palladacycle is shown to be a highly efficient catalyst for the formation of N-substituted benzylic stereocenters; t

C 1-symmetric dicyclopentadienes as new chiral diene ligands for asymmetric rhodium-catalyzed arylation of N-tosylarylimines

Monosubstituted C1-symmetric dicyclopentadienes as a new class of diene ligands have been developed for asymmetric arylation of N-tosylarylimines in excellent yields (98-99%) with high enantioselectivities (90-96%). The preparation of these diene ligands relied on an efficient lipase-catalyzed resolution as the key step.