Cas 155375-38-5,2, 5-diamino-7-(methylthio)-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-6-carbonitrile

155375-38-5

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Basic information

Product Name: 2, 5-diamino-7-(methylthio)-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-6-carbonitrile
Synonyms: 2, 5-diamino-7-(methylthio)-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-6-carbonitrile
CAS NO:155375-38-5
Molecular Formula:
Molecular Weight: 324.369
EINECS: N/A
Product Categories: N/A
Mol File: 155375-38-5.mol
Article Data: 2

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, 5-diamino-7-(methylthio)-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-6-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2, 5-diamino-7-(methylthio)-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-6-carbonitrile(155375-38-5)
EPA Substance Registry System: 2, 5-diamino-7-(methylthio)-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-6-carbonitrile(155375-38-5)

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: 155375-38-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155375-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,7 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155375-38:
(8*1)+(7*5)+(6*5)+(5*3)+(4*7)+(3*5)+(2*3)+(1*8)=145
145 % 10 = 5
So 155375-38-5 is a valid CAS Registry Number.

155375-38-5Upstream product

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155375-38-5Relevant articles and documents

A First Microwave-Assisted Synthesis of a New Class of Purine and Guanine Thioglycoside Analogs

Elgemeie, Galal,Abu-Zaied, Mamdouh,Hebishy, Ali,Abbas, Nermen,Hamed, Mai

, p. 459 - 478 (2016)

A first microwave-assisted synthesis of a new class of novel purine thioglycoside analogs from readily available starting materials has been described. The key step of this protocol is the formation of sodium pyrazolo[1,5-a]pyrimidine-7-thiolate and 7-mer

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