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4-(Piperidine-1-carbonyl)benzenesulfonamide is a chemical compound with the molecular formula C12H16N2O3S. It is a white crystalline solid that belongs to the class of sulfonamide derivatives. 4-(piperidine-1-carbonyl)benzenesulfonamide is characterized by the presence of a benzene ring with a sulfonamide group attached at the 4-position, and a piperidine-1-carbonyl group connected to the same benzene ring. It is synthesized through the reaction of 4-aminobenzenesulfonamide with piperidine-1-carboxylic acid, and is used as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Due to its potential applications in the synthesis of drugs and other chemical products, 4-(piperidine-1-carbonyl)benzenesulfonamide is an important compound in the field of organic chemistry.

4302-78-7

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4302-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4302-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,0 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4302-78:
(6*4)+(5*3)+(4*0)+(3*2)+(2*7)+(1*8)=67
67 % 10 = 7
So 4302-78-7 is a valid CAS Registry Number.

4302-78-7Downstream Products

4302-78-7Relevant academic research and scientific papers

Benzamide-4-sulfonamides are effective human carbonic anhydrase I, II, VII, and IX inhibitors

Abdoli, Morteza,Bozdag, Murat,Angeli, Andrea,Supuran, Claudiu T.

, (2018)

A series of benzamides incorporating 4-sulfamoyl moieties were obtained by reacting 4-sulfamoyl benzoic acid with primary and secondary amines and amino acids. These sulfonamides were investigated as inhibitors of the metalloenzyme carbonic anhydrase (CA,

Seeking new approach for therapeutic treatment of cholera disease via inhibition of bacterial carbonic anhydrases: experimental and theoretical studies for sixteen benzenesulfonamide derivatives

Gitto, Rosaria,De Luca, Laura,Mancuso, Francesca,Del Prete, Sonia,Vullo, Daniela,Supuran, Claudiu T.,Capasso, Clemente

, p. 1186 - 1192 (2019)

A series of sixteen benzenesulfonamide derivatives has been synthesised and tested as inhibitors of Vibrio cholerae carbonic anhydrase (CA) enzymes, belonging to α-CA, β-CA, and γ-CA classes (VchCAα, VchCAβ, and VchCAγ). The determined Ki value

Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety

Buemi, Maria Rosa,Di Fiore, Anna,De Luca, Laura,Angeli, Andrea,Mancuso, Francesca,Ferro, Stefania,Monti, Simona Maria,Buonanno, Martina,Russo, Emilio,De Sarro, Giovanbattista,De Simone, Giuseppina,Supuran, Claudiu T.,Gitto, Rosaria

, p. 443 - 452 (2018/12/13)

Guided by the crystal structure of 4-(3,4-dihydroquinolin-1(2H)-ylcarbonyl)benzenesulfonamide 3 in complex with hCA II (PDB code 4Z0Q), a novel series of cycloalkylamino-1-carbonylbenzenesulfonamides was designed and synthesized. Thus, we replaced the qui

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