Cas 1402041-64-8,2-(3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)-N-(phenylsulfonyl)acetamide

1402041-64-8

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Basic information

Product Name: 2-(3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)-N-(phenylsulfonyl)acetamide
Synonyms: 2-(3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)-N-(phenylsulfonyl)acetamide
CAS NO:1402041-64-8
Molecular Formula:
Molecular Weight: 486.378
EINECS: N/A
Product Categories: N/A
Mol File: 1402041-64-8.mol
Article Data: 1

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-(3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)-N-(phenylsulfonyl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)-N-(phenylsulfonyl)acetamide(1402041-64-8)
EPA Substance Registry System: 2-(3-(4-chlorophenyl)-1-phenyl-1H-pyrazol-4-yl)-N-(phenylsulfonyl)acetamide(1402041-64-8)

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: 1402041-64-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1402041-64-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,0,4 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1402041-64:
(9*1)+(8*4)+(7*0)+(6*2)+(5*0)+(4*4)+(3*1)+(2*6)+(1*4)=88
88 % 10 = 8
So 1402041-64-8 is a valid CAS Registry Number.

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1402041-64-8Relevant articles and documents

Modified acidic nonsteroidal anti-inflammatory drugs as dual inhibitors of mPGES-1 and 5-LOX

Elkady, Mahmoud,Niess, Raimund,Bauer, Julia,Luderer, Susann,Ambrosi, Giulia,Laufer, Stefan A.,Schaible, Anja M.,Werz, Oliver

supporting information, p. 8958 - 8962,5 (2020/09/16)

mPGES-1 is a promising target for development of new anti-inflammatory drugs. We aimed to create mPGES-1 inhibitors by modifying the structure of NSAIDs by replacing the carboxylic acid functionality by sulfonamide moieties. Compounds were also tested for

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