854637-14-2

Basic information

• Product Name: N-benzyl-4-methyl-N-phenethylbenzenesulfonamide
• Synonyms: N-benzyl-4-methyl-N-phenethylbenzenesulfonamide
• CAS NO: 854637-14-2
• Molecular Weight: 365.496
• Mol File: 854637-14-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyl-4-methyl-N-phenethylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-4-methyl-N-phenethylbenzenesulfonamide(854637-14-2)
• EPA Substance Registry System: N-benzyl-4-methyl-N-phenethylbenzenesulfonamide(854637-14-2)

Safety Data

• Hazardous Substances Data: 854637-14-2(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 5450-75-9 4-methyl-N-(2-phenylethyl)benzenesulfonamide 
• 100-39-0 benzyl bromide 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 1576-37-0 N-benzyl-p-toluenesulfonamide 
• 609769-63-3 N-benzyl-N-(p-toluenesulfonyl)-2-phenylethynylamine 
• 1617518-96-3 (Z)-N-benzyl-N-[2-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethenyl]-4-methylbenzenesulfonamide 
• 854637-27-7 N-benzyl-N-(β-bromo-phenethyl)-toluene-4-sulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 100-46-9 benzylamine 
• 103-63-9 1-phenyl-2-bromoethane 

Downstream Products

• 3647-71-0 N-benzyl-2-phenylethylamine 

Relevant articles and documents

Enantioselective Rhodium-Catalyzed Hydrogenation of (Z)-N-Sulfonyl-α-dehydroamido Boronic Esters

Highly enantioselective rhodium-catalyzed hydrogenation of (Z)-N-sulfonyl-α-dehydroamido boronic esters is realized for the first time using a JosiPhos-type ligand. This method has enabled convenient synthesis of a series of enantio-enriched N-sulfonyl-α-amido boronic esters in good yields and excellent enantioselectivities (up to 99% ee).

Hg cathode-free electrochemical detosylation of N,N-disubstituted p-toluenesulfonamides: mild, efficient, and selective removal of N-tosyl group

Hg cathode-free electrochemical detosylation of N,N-disubstituted p-toluenesulfonamides was successfully carried out by a constant current electrolysis using an undivided cell equipped with a platinum cathode and a magnesium anode in the presence of an arene mediator. The deprotection proceeded efficiently and selectively under neutral and mild conditions with a stoichiometric amount of electricity without the use of an Hg cathode to obtain the corresponding secondary amines in good to excellent yields.