Cas 1262236-40-7,7-phenyl-3-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylthio)-7H-pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine

1262236-40-7

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Basic information

Product Name: 7-phenyl-3-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylthio)-7H-pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine
Synonyms:
CAS NO:1262236-40-7
Molecular Formula:
Molecular Weight: 462.497
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-phenyl-3-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylthio)-7H-pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 7-phenyl-3-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylthio)-7H-pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine(1262236-40-7)
EPA Substance Registry System: 7-phenyl-3-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylthio)-7H-pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine(1262236-40-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1262236-40-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262236-40-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,2,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1262236-40:
(9*1)+(8*2)+(7*6)+(6*2)+(5*2)+(4*3)+(3*6)+(2*4)+(1*0)=127
127 % 10 = 7
So 1262236-40-7 is a valid CAS Registry Number.

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1262236-40-7Relevant academic research and scientific papers

Synthesis of new sulfur-linked 1,2,4-triazolothienopyrimidine and 1,2,4-triazolopyrazolopyrimidine derivatives containing fused heterocyclic pyrimidines

Song, Yang-Heon,Son, Hoon Young

, p. 1183 - 1187 (2010)

(Chemical Equation Presented) A series of novel bis-heterocyclic compounds 12-20 were synthesized by integrating fused heterocyclic pyrimidines, such as thienopyrimidine and pyrazolopyrimidine into the scaffold of thienotriazolopyrimidines, and pyrazolotriazolopyrimidines through a sulfur-linkage.

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