Cas 1365659-26-2,3-cyano-6-phenyl-7-(2-hydroxyl-4-methoxy-6-methylphenyl)pyrazolo[1,5-a]pyrimidine

1365659-26-2

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Basic information

Product Name: 3-cyano-6-phenyl-7-(2-hydroxyl-4-methoxy-6-methylphenyl)pyrazolo[1,5-a]pyrimidine
Synonyms: 3-cyano-6-phenyl-7-(2-hydroxyl-4-methoxy-6-methylphenyl)pyrazolo[1,5-a]pyrimidine
CAS NO:1365659-26-2
Molecular Formula:
Molecular Weight: 356.384
EINECS: N/A
Product Categories: N/A
Mol File: 1365659-26-2.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: 3-cyano-6-phenyl-7-(2-hydroxyl-4-methoxy-6-methylphenyl)pyrazolo[1,5-a]pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 3-cyano-6-phenyl-7-(2-hydroxyl-4-methoxy-6-methylphenyl)pyrazolo[1,5-a]pyrimidine(1365659-26-2)
EPA Substance Registry System: 3-cyano-6-phenyl-7-(2-hydroxyl-4-methoxy-6-methylphenyl)pyrazolo[1,5-a]pyrimidine(1365659-26-2)

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: 1365659-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1365659-26-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,6,5 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1365659-26:
(9*1)+(8*3)+(7*6)+(6*5)+(5*6)+(4*5)+(3*9)+(2*2)+(1*6)=192
192 % 10 = 2
So 1365659-26-2 is a valid CAS Registry Number.

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1365659-26-2Relevant articles and documents

Simple and efficient method for synthesis of 3-cyano-6,7-diarylpyrazolo[1, 5-a]pyrimidine from isoflavones

Ma, Yu-Qing,Zhang, Zun-Ting,He, Qing,Xue, Dong,Zhang, Peng-Fei

experimental part, p. 933 - 941 (2012/02/01)

A series of 3-cyano-6,7-diarylpyrazolo[1,5-a]pyrimidines have been synthesized directly from the 5-amino-4-cyano-1H-pyrazole and isoflavones. The target compound was obtained by a condensation reaction. Structures of compounds were demonstrated by Fourier

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