75159-10-3

Basic information

• Product Name: 4-METHYL-N-(4-METHYL-BENZYLIDENE)-BENZENESULFONAMIDE
• Synonyms: 4-METHYL-N-(4-METHYL-BENZYLIDENE)-BENZENESULFONAMIDE;N-(4-Methylbenzylidene)-4-MethylbenzenesulfonaMide
• CAS NO: 75159-10-3
• Molecular Formula: C₁₅H₁₅NO₂S
• Molecular Weight: 273.35
• Mol File: 75159-10-3.mol
• Article Data: 98

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-METHYL-N-(4-METHYL-BENZYLIDENE)-BENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-N-(4-METHYL-BENZYLIDENE)-BENZENESULFONAMIDE(75159-10-3)
• EPA Substance Registry System: 4-METHYL-N-(4-METHYL-BENZYLIDENE)-BENZENESULFONAMIDE(75159-10-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• Hazardous Substances Data: 75159-10-3(Hazardous Substances Data)

Upstream product

• 10504-92-4 N-p-xylyl-p-toluenesulfonamide 
• 589-18-4 4-Methylbenzyl alcohol 
• 70-55-3 toluene-4-sulfonamide 
• 73844-91-4 (2S,3S)-2-(Toluene-4-sulfonyl)-3-p-tolyl-oxaziridine 
• 603-35-0 triphenylphosphine 
• 104-87-0 4-methyl-benzaldehyde 
• 101359-08-4 N-tosyltriphenylbismuthimine 
• 63609-88-1 9-fluorenethione S-p-toluenesulfomimide 
• 4702-76-5 N-[1-p-Tolyl-meth-(Z)-ylidene]-N'-[1-p-tolyl-meth-(E)-ylidene]-hydrazine 
• 622-58-2 p-Tolylisocyanate 
• 18869-30-2 (E)-4,4'-dibromostilbene 
• 1588-49-4 4,4'-dimethylstilbene 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 4083-64-1 Tosyl isocyanate 

Downstream Products

• 10504-92-4 N-p-xylyl-p-toluenesulfonamide 
• 153529-45-4 (E)-diethyl 1-ethoxycarbonyl-2-(4-methylphenyl)-vinylphosphonate 
• 51146-24-8 (E)-diethyl 1-cyano-2-(4-methylphenyl)-vinylphosphonate 
• 243671-17-2 4-methyl-N-(1-p-tolylbut-3-enyl)benzenesulfonamide 

Relevant articles and documents

Catalytic Asymmetric Hydroacyloxylation/Ring-Opening Reaction of Ynamides, Acids, and Aziridines

A highly enantioselective three-component reaction of ynamides with carboxylic acids and 2,2′-diester aziridines has been realized by using a chiral N,N′-dioxide/Ho(OTf)3 complex as a Lewis acid catalyst. The process includes the formation of an α-acyloxyenamide intermediate through the addition of carboxylic acids to ynamides and the following enantioselective nucleophilic addition to in-situ-generated azomethine ylides induced by the chiral catalyst. A range of amino acyloxyenamides are delivered in moderate to good yields with good ee values. In addition, a possible catalytic cycle with a transition model is proposed to elucidate the reaction mechanism.

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,

Copper-boryl mediated transfer hydrogenation of N-sulfonyl imines using methanol as the hydrogen donor

B2Pin2-assisted copper-catalyzed transfer hydrogenation of aromatic sulfonylimines has been achieved, delivering a variety of aryl/heteroaryl sulfonamides in good to excellent yields under mild reaction conditions and with methanol a