3157-65-1

Basic information

• Product Name: N-(4-Chlorobenzylidene)-4-methylbenzenesulfonamide
• Synonyms: N-(4-Chlorobenzylidene)-4-methylbenzenesulfonamide;(NZ)-N-[(4-chlorophenyl)methylidene]-4-methylbenzenesulfonamide
• CAS NO: 3157-65-1
• Molecular Formula: C₁₄H₁₂ClNO₂S
• Molecular Weight: 293.76858
• Product Categories: Building Blocks;Chemical Synthesis;Imines/Amidines;Nitrogen Compounds;Organic Building Blocks;Sulfonamides/Sulfinamides;Sulfur Compounds
• Mol File: 3157-65-1.mol
• Article Data: 82

Chemical Properties

• Melting Point: 175-180℃
• Appearance: /
• CAS DataBase Reference: N-(4-Chlorobenzylidene)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Chlorobenzylidene)-4-methylbenzenesulfonamide(3157-65-1)
• EPA Substance Registry System: N-(4-Chlorobenzylidene)-4-methylbenzenesulfonamide(3157-65-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• Hazardous Substances Data: 3157-65-1(Hazardous Substances Data)

Upstream product

• 941-55-9 4-toluenesulfonyl azide 
• 104-88-1 4-chlorobenzaldehyde 
• 101359-08-4 N-tosyltriphenylbismuthimine 
• 69900-95-4 2-(p-toluenesulfonyl)-3-(p-chlorophenyl)oxaziridine 
• 2403-61-4 p-chlorobenzaldehyde diethyl acetal 
• 70-55-3 toluene-4-sulfonamide 
• 1058-14-6 N-p-tolylsulfonylphosphine imide 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 3395-81-1 4-chlorobenzaldehyde dimethyl acetal 
• 127-65-1 chloroamine-T 
• 873-76-7 para-Chlorobenzyl alcohol 
• 4083-64-1 Tosyl isocyanate 
• 10504-98-0 N-(4-chlorobenzyl)-p-toluenesulfonamide 

Downstream Products

• 221000-81-3 (4R,5R)-cis-4-(ethoxycarbonyl)-5-(4-chlorophenyl)-1-N-tosyl-2-imidazoline 
• 228702-93-0 (4S,5S)-cis-4-(ethoxycarbonyl)-5-(4-chlorophenyl)-1-N-tosyl-2-imidazoline 
• 53235-79-3 (E)-diethyl 1-ethoxycarbonyl-2-(4-chlorophenyl)-vinylphosphonate 
• 439077-74-4 N-[1'-(4''-chlorophenyl)-2'-methylene-3'-oxobutyl]-4-methylbenzenesulfonamide 
• 452897-59-5 N-[[1-(tert-butyldimethylsilanyl)-1H-indol-3-yl]-(4-chlorophenyl)methyl]-4-methylbenzenesulfonamide 

Relevant articles and documents

Copper(II) triflate-catalyzed and tosyl isocyanate-mediated three-step tandem synthesis of 9-arylfluorenes

A Cu(OTf)2-catalyzed and TsNCO-mediated three-step tandem synthesis of 9-arylfluorenes were developed from biphenyls and aryl aldehydes, by which the electron-poor 9-aryl substituted fluorenes were synthesized smoothly. Its success is mainly at

Facile synthesis, antimicrobial and antiviral evaluation of novel substituted phenyl 1,3-thiazolidin-4-one sulfonyl derivatives

A series of novel substituted phenyl 1, 3-thiazolidin-4-one sulfonyl derivatives 5 (a-t) were synthesized and screened for their in-vitro anti-microbial and anti-viral activity. The result of the anti-microbial assay demonstrated compounds 5d, 5f, 5g, 5h,

Reductive alkylation of imines via asymmetric Cu-catalyzed addition of organozirconium reagents

Chiral amines are important as medicines or agrochemicals. They are often assembled by nucleophilic addition to corresponding compounds featuring C[dbnd]N bond. Pre-made organometallics are typical nucleophiles in this reaction. In this work, we describe