Cas 304648-12-2,{2-(2,5-dimethyl-pyrrole-1-sulfonyl)-5-[5-(4-methoxy-phenyl)-3-trifluoromethyl-pyrazol-1-yl]-phenyl}-methanol

304648-12-2

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Basic information

Product Name: {2-(2,5-dimethyl-pyrrole-1-sulfonyl)-5-[5-(4-methoxy-phenyl)-3-trifluoromethyl-pyrazol-1-yl]-phenyl}-methanol
Synonyms:
CAS NO:304648-12-2
Molecular Formula:
Molecular Weight: 505.518
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: {2-(2,5-dimethyl-pyrrole-1-sulfonyl)-5-[5-(4-methoxy-phenyl)-3-trifluoromethyl-pyrazol-1-yl]-phenyl}-methanol(CAS DataBase Reference)
NIST Chemistry Reference: {2-(2,5-dimethyl-pyrrole-1-sulfonyl)-5-[5-(4-methoxy-phenyl)-3-trifluoromethyl-pyrazol-1-yl]-phenyl}-methanol(304648-12-2)
EPA Substance Registry System: {2-(2,5-dimethyl-pyrrole-1-sulfonyl)-5-[5-(4-methoxy-phenyl)-3-trifluoromethyl-pyrazol-1-yl]-phenyl}-methanol(304648-12-2)

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: 304648-12-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 304648-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,6,4 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 304648-12:
(8*3)+(7*0)+(6*4)+(5*6)+(4*4)+(3*8)+(2*1)+(1*2)=122
122 % 10 = 2
So 304648-12-2 is a valid CAS Registry Number.

304648-12-2Upstream product

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304648-12-2Relevant academic research and scientific papers

Polar substitutions in the benzenesulfonamide ring of celecoxib afford a potent 1,5-diarylpyrazole class of COX-2 inhibitors

Singh, Sunil K.,Reddy, P. Ganapati,Rao, K. Srinivasa,Lohray, Braj B.,Misra,Rajjak, Shaikh A.,Rao, Yeleswarapu K.,Venkateswarlu

, p. 499 - 504 (2004)

Several chemical modifications in the N1-benzenesulfonamide ring of celecoxib are presented. The series with a hydroxymethyl group adjacent to the sulfonamide was found to be the most potent modification that yielded many compounds selectively active against COX-2 enzyme in vitro.

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