Cas 1242771-83-0,7-(4-chlorophenyl)-4,7-dihydro-N-(4-methoxyphenyl)-5-methyl-3-phenyl[1,2,3]triazolo[1,5-a]pyrimidine-6-carboxamide

1242771-83-0

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Basic information

Product Name: 7-(4-chlorophenyl)-4,7-dihydro-N-(4-methoxyphenyl)-5-methyl-3-phenyl[1,2,3]triazolo[1,5-a]pyrimidine-6-carboxamide
Synonyms:
CAS NO:1242771-83-0
Molecular Formula:
Molecular Weight: 471.946
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: 7-(4-chlorophenyl)-4,7-dihydro-N-(4-methoxyphenyl)-5-methyl-3-phenyl[1,2,3]triazolo[1,5-a]pyrimidine-6-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 7-(4-chlorophenyl)-4,7-dihydro-N-(4-methoxyphenyl)-5-methyl-3-phenyl[1,2,3]triazolo[1,5-a]pyrimidine-6-carboxamide(1242771-83-0)
EPA Substance Registry System: 7-(4-chlorophenyl)-4,7-dihydro-N-(4-methoxyphenyl)-5-methyl-3-phenyl[1,2,3]triazolo[1,5-a]pyrimidine-6-carboxamide(1242771-83-0)

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: 1242771-83-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242771-83-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,7,7 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1242771-83:
(9*1)+(8*2)+(7*4)+(6*2)+(5*7)+(4*7)+(3*1)+(2*8)+(1*3)=150
150 % 10 = 0
So 1242771-83-0 is a valid CAS Registry Number.

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1242771-83-0Relevant academic research and scientific papers

Efficient multicomponent synthesis of highly substituted [1,2,3]triazolo[1,5-a]pyrimidines

Gladkov, Eugene S.,Sirko, Svetlana N.,Shishkina, Svetlana V.,Shishkin, Oleg V.,Knyazeva, Irina V.,Desenko, Sergey M.,Chebanov, Valentin A.

experimental part, p. 773 - 779 (2011/06/28)

An efficient and facile multicomponent procedure for the synthesis of highly substituted [1,2,3]triazolo-[1,5-a]pyrimidines by reaction of equimolar amounts of aromatic aldehyde, CH-acid, and 5-amino-1,2,3-triazole in refluxing dimethylformamide is described. Springer-Verlag 2010.

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