172426-19-6

Basic information

• Product Name: N-(4-cyano-2-nitrophenyl)-4-methylbenzenesulfonamide
• Synonyms: N-(4-cyano-2-nitrophenyl)-4-methylbenzenesulfonamide
• CAS NO: 172426-19-6
• Molecular Weight: 317.325
• Mol File: 172426-19-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-(4-cyano-2-nitrophenyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-cyano-2-nitrophenyl)-4-methylbenzenesulfonamide(172426-19-6)
• EPA Substance Registry System: N-(4-cyano-2-nitrophenyl)-4-methylbenzenesulfonamide(172426-19-6)

Safety Data

• Hazardous Substances Data: 172426-19-6(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 6393-40-4 4-Amino 3-nitro-benzonitrile 
• 1009-35-4 4-fluoro-3-nitrobenzonitrile 
• 70-55-3 toluene-4-sulfonamide 
• 873-74-5 4-Aminobenzonitrile 
• 56768-53-7 N-(4-cyanophenyl)-4-methylbenzenesulfonamide 

Downstream Products

• 172426-20-9 N-(2-amino-4-cyanophenyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

A microwave-assisted approach to N-(2-nitrophenyl)benzenesulfonamides that enhanced peroxidase activity in response to excess cadmium

A facile and efficient approach to N-(2-nitrophenyl) benzenesulfonamides was developed under microwave irradiation. A series of pyrabactin analogues containing nitrophenyl scaffold was obtained in excellent yields. In addition, the method was pretty suitable to prepare flusulfamide. Significantly, the 3ae could enhance POD activity in response to heavy metal stress.

Chemoselective nitration of aromatic sulfonamides with tert-butyl nitrite

A methodology for the efficient conversion of aromatic sulfonamides into their mono-nitro derivatives using tert-butyl nitrite is reported. The reaction exhibits a high degree of chemoselectivity for sulfonamide functionalized aryl systems, even in the presence of other sensitive or potentially reactive functionalities.

SULFONAMIDE DERIVATIVES

The present invention relates to microbicides for agricultural or horticultural use containing sulfonamide derivative of, for example, a formula (I):or a salt thereof,[wherein A1is (1) an aryl group which may be substituted or (2) a heterocyclic group which may be substituted, X1is (1) a chemical bond, (2) a methylene group which may be substituted, or (3) a vinylene group which may be substituted, B1is a five-membered heterocyclic group comprising nitrogen or sulfur atoms as the ring-constructing atoms except for carbon atoms and may be substituted or a condensed heterocyclic group which may be substituted, Z1is (1) a hydrocarbon group which may be substituted, (2) an acyl group which may be substituted, (3) formyl group, (4) an amino group which may be substituted, (5) a group represented by -N=CR1R2(wherein each of R1and R2is a hydrogen atom or a hydrocarbon group which may be substituted), (6) a cyclic amino group, (7) a group represented by -OR3(wherein R3is a hydrogen atom, a hydrocarbon group which may be substituted, an acyl group which may be substituted, formyl group or an alkylsulfonyl group which may be substituted) or (8) -S(O)nR4(wherein n stands for an integer from 0 to 2, R4stands for a hydrogen atom or a hydrocarbon group which may be substituted). The said compounds or the salts thereof are sulfonamide derivatives with microbicidal action, areuseful as excellent microbicides for agricultural or horticultural use, because they are safe, and they have little influence on human beings, farm animals, natural enemies, or the environment, and exert excellent control effects even on resistant microbes.