13707-46-5

Basic information

• Product Name: Benzenesulfonamide, 4-methyl-N-[(4-nitrophenyl)methylene]-
• CAS NO: 13707-46-5
• Molecular Formula: C14H12N2O4S
• Molecular Weight: 304.326
• Mol File: 13707-46-5.mol
• Article Data: 71

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-[(4-nitrophenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-[(4-nitrophenyl)methylene]-(13707-46-5)
• EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-[(4-nitrophenyl)methylene]-(13707-46-5)

Safety Data

• Hazardous Substances Data: 13707-46-5(Hazardous Substances Data)

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 70-55-3 toluene-4-sulfonamide 
• 941-55-9 4-toluenesulfonyl azide 
• 4104-47-6 N-sulfinyl-p-toluenesulfonamide 
• 1058-14-6 N-p-tolylsulfonylphosphine imide 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 67490-46-4 4-nitrobenzaldehyde 
• 619-73-8 4-nitrobenzyl chloride 
• 62486-35-5 Te,Te-di(p-methoxyphenyl)-N-(p-tolylsulfonyl)tellurimide 
• 672-78-6 methyl p-toluene sulfinate 
• 6873-55-8 p-tolylsulfinyl amide 
• 103-19-5 di(p-tolyl) disulfide 
• 728882-12-0 4-Methyl-benzenesulfinic acid 1-(4-nitro-phenyl)-meth-(E)-ylideneamide 
• 127-65-1 chloroamine-T 

Downstream Products

• 130231-96-8 (2S,3R)-4,4-Dimethyl-2-(4-nitro-phenyl)-5-oxo-1-(toluene-4-sulfonyl)-pyrrolidine-3-carboxylic acid ethyl ester 
• 130231-96-8 (2S,3S)-4,4-Dimethyl-2-(4-nitro-phenyl)-5-oxo-1-(toluene-4-sulfonyl)-pyrrolidine-3-carboxylic acid ethyl ester 
• 73844-95-8 (2S,3S)-3-(4-Nitro-phenyl)-2-(toluene-4-sulfonyl)-oxaziridine 
• 73844-95-8 3-(4-nitrophenyl)-2-p-tolylsulfonyloxaziridine 
• 79807-52-6 acetic acid 
• 103298-41-5 1-methyl-4-(4-nitrophenyl)-1H-imidazole 
• 38980-93-7 5-(4-nitrophenyl)-1H-imidazole 

Relevant articles and documents

HAMMETT INVESTIGATION OF IODIDE-ION-INDUCED DEOXYGENATIVE REDUCTION OF 2-ARYL'SULPHONYL-3 ARYLOXAZIRIDINES IN METHANOL-WATER (50percent v/v)

The Hammett substituent dependence of the iodide ion induced deoxygenation of 2-aryl'sulphonyl-3-aryloxaziridines, in aqu. methanol suggests that the reaction proceeds by nucleophilic attack on oxygen with concomitant O-N bond breakage.

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

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,

TfOH-catalyzed formal [3+2] cycloaddition of N-tosylaziridine dicarboxylates and nitriles: Synthesis of tetrafunctionalized 2-imidazolines

We developed an efficient method for synthesis of tetrafunctionalized 2-imidazolines using TfOH-catalyzed formal [3+2] cycloaddition of N-tosylaziridine dicarboxylates and nitriles. This is the first report of C–N bond cleavage of N-tosylaziridine dicarboxylates catalyzed by Br?nsted acid and the reaction worked well over wide scope of substrates in good to excellent yields under mild conditions. The method has the potential to be applied to pharmaceutical design and synthesis of tetrafunctionalized 2-imidazolines.