Cas 951900-76-8,N-[5-(3-chlorobenzyl)-1,3-thiazol-2-yl]-5-methyl-1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxamide

951900-76-8

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Basic information

Product Name: N-[5-(3-chlorobenzyl)-1,3-thiazol-2-yl]-5-methyl-1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxamide
Synonyms:
CAS NO:951900-76-8
Molecular Formula:
Molecular Weight: 423.926
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: N-[5-(3-chlorobenzyl)-1,3-thiazol-2-yl]-5-methyl-1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[5-(3-chlorobenzyl)-1,3-thiazol-2-yl]-5-methyl-1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxamide(951900-76-8)
EPA Substance Registry System: N-[5-(3-chlorobenzyl)-1,3-thiazol-2-yl]-5-methyl-1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxamide(951900-76-8)

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: 951900-76-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 951900-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,9,0 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 951900-76:
(8*9)+(7*5)+(6*1)+(5*9)+(4*0)+(3*0)+(2*7)+(1*6)=178
178 % 10 = 8
So 951900-76-8 is a valid CAS Registry Number.

951900-76-8Upstream product

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951900-76-8Relevant academic research and scientific papers

Synthesis and anticancer activity evaluation of new 1,2,3-triazole-4- carboxamide derivatives

Pokhodylo, Nazariy,Shyyka, Olga,Matiychuk, Vasyl

, p. 2426 - 2438 (2014/05/06)

Anticancer screening of several novel 1,2,3-triazoles has been performed. The 1,2,3-triazole derivatives were synthesized from available starting materials according to the convenient synthetic procedures using a multicomponent reaction which gave a wide

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