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 
• 73844-95-8 (2S,3S)-3-(4-Nitro-phenyl)-2-(toluene-4-sulfonyl)-oxaziridine 
• 2403-62-5 p-nitrobenzaldehyde diethyl acetal 
• 1058-14-6 N-p-tolylsulfonylphosphine imide 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 98-10-2 benzenesulfonamide 
• 104-88-1 4-chlorobenzaldehyde 
• 127-65-1 chloroamine-T 
• 67490-46-4 4-nitrobenzaldehyde 
• 619-73-8 4-nitrobenzyl chloride 
• 62486-35-5 Te,Te-di(p-methoxyphenyl)-N-(p-tolylsulfonyl)tellurimide 

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.

One-Pot Synthesis of Diazirines and 15N2-Diazirines from Ketones, Aldehydes and Derivatives: Development and Mechanistic Insight

Broad scope one-pot diazirine synthesis strategies have been developed using two different oxidants depending on the nature of the starting material. In all cases, an inexpensive commercial solution of ammonia (NH3) in methanol (MeOH) was emplo

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

Synthesis and biological evaluation of substituted phenyl azetidine-2-one sulphonyl derivatives as potential antimicrobial and antiviral agents

In the present study, we intend to synthesize a series of novel substituted phenyl azetidine-2-one sulphonyl derivatives. The entire set of derivatives 5 (a-t) were screened for in-vitro antibacterial, and antifungal activity, and among them eleven compou