Cas 1353056-01-5,2-[5-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-1,3-benzothiazole-6-sulfonamide

1353056-01-5

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Basic information

Product Name: 2-[5-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-1,3-benzothiazole-6-sulfonamide
Synonyms: 2-[5-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-1,3-benzothiazole-6-sulfonamide
CAS NO:1353056-01-5
Molecular Formula:
Molecular Weight: 454.453
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-[5-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-1,3-benzothiazole-6-sulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-[5-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-1,3-benzothiazole-6-sulfonamide(1353056-01-5)
EPA Substance Registry System: 2-[5-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]-1,3-benzothiazole-6-sulfonamide(1353056-01-5)

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: 1353056-01-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1353056-01-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,0,5 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1353056-01:
(9*1)+(8*3)+(7*5)+(6*3)+(5*0)+(4*5)+(3*6)+(2*0)+(1*1)=125
125 % 10 = 5
So 1353056-01-5 is a valid CAS Registry Number.

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1353056-01-5Relevant academic research and scientific papers

Heteroaromatic analogues of 1,5-diarylpyrazole class as anti-inflammatory agents

Sharma, Pawan K.,Chandna, Nisha,Kumar, Surender,Kmar, Pawan,Kumar, Satish,Kaushik, Pawan,Kaushik, Dhirender

, p. 3757 - 3766 (2013/02/23)

A novel series of heteroaromatic analogues of known anti-inflammatory (AI) drug celecoxib replacing the benzenesulfonamide moiety with 6- sulfonamidobenzothiazol-2-yl moiety was synthesized. Regioselective synthesis of the target compounds 2a-i having 1,5

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