Cas 356561-57-4,4-({[(4-chlorophenyl)amino]carbonyl}amino)-N-(5-methyl-3-isoxazolyl)benzenesulfonamide

356561-57-4

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Basic information

Product Name: 4-({[(4-chlorophenyl)amino]carbonyl}amino)-N-(5-methyl-3-isoxazolyl)benzenesulfonamide
Synonyms: 4-({[(4-chlorophenyl)amino]carbonyl}amino)-N-(5-methyl-3-isoxazolyl)benzenesulfonamide;4-{[(4-chlorophenyl)carbamoyl]amino}-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide
CAS NO:356561-57-4
Molecular Formula: C17H15ClN4O4S
Molecular Weight: 406.8434
EINECS: N/A
Product Categories: N/A
Mol File: 356561-57-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: 1.545±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 5.63±0.50(Predicted)
CAS DataBase Reference: 4-({[(4-chlorophenyl)amino]carbonyl}amino)-N-(5-methyl-3-isoxazolyl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-({[(4-chlorophenyl)amino]carbonyl}amino)-N-(5-methyl-3-isoxazolyl)benzenesulfonamide(356561-57-4)
EPA Substance Registry System: 4-({[(4-chlorophenyl)amino]carbonyl}amino)-N-(5-methyl-3-isoxazolyl)benzenesulfonamide(356561-57-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 356561-57-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 356561-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,5,6 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 356561-57:
(8*3)+(7*5)+(6*6)+(5*5)+(4*6)+(3*1)+(2*5)+(1*7)=164
164 % 10 = 4
So 356561-57-4 is a valid CAS Registry Number.

356561-57-4Upstream product

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356561-57-4Relevant academic research and scientific papers

Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors

Mishra, Chandra Bhushan,Kumari, Shikha,Angeli, Andrea,Monti, Simona Maria,Buonanno, Martina,Prakash, Amresh,Tiwari, Manisha,Supuran, Claudiu T.

, p. 174 - 179 (2016)

A series of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamide derivatives has been designed, synthesized and screened for their in vitro human carbonic anhydrase (hCA; EC 4.2.1.1) inhibition potential. These

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