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1,2,3-Triazolo[1,5-a]pyrazine is a heterocyclic compound characterized by a fused ring structure consisting of a triazole and a pyrazine. [1,2,3]Triazolo[1,5-a]pyrazine is notable for its potential applications in medicinal chemistry, particularly as a scaffold in the design of novel drugs. The triazole ring, with its nitrogen-rich structure, contributes to the compound's stability and reactivity, while the pyrazine ring adds an additional layer of complexity and functionality. Research into 1,2,3-triazolo[1,5-a]pyrazine and its derivatives often focuses on exploring their biological activities, such as antimicrobial, anticancer, and antiviral properties, making them a subject of interest for the development of new therapeutic agents.

51392-75-7

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51392-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51392-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,9 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51392-75:
(7*5)+(6*1)+(5*3)+(4*9)+(3*2)+(2*7)+(1*5)=117
117 % 10 = 7
So 51392-75-7 is a valid CAS Registry Number.

51392-75-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name triazolo[1,5-a]pyrazine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51392-75-7 SDS

51392-75-7Downstream Products

51392-75-7Relevant academic research and scientific papers

4-Pyridylnitrene and 2-pyrazinylcarbene

Wentrup, Curt,Reisinger, Ales,Kvaskoff, David

, p. 754 - 760 (2013/06/27)

Both flash vacuum thermolysis (FVT) and matrix photolysis generate 2-diazomethylpyrazine (22) from 1,2,3-triazolo[1,5- a]pyrazine (24). FVT of 4-azidopyridine (18) as well as of 24 or 2-(5-tetrazolyl)pyrazine (23) affords the products expected from the nitrene, i.e., 4,4'-azopyridine and 2- and 3-cyanopyrroles. Matrix photolyses of both 18 and 24 result in ring expansion of 4-pyridylnitrene/2-pyrazinylcarbene to 1,5-diazacyclohepta-1,2,4,6-tetraene (20). Further photolysis causes ring opening to the ketenimine 27.

1,2,3-TRIAZOLOAZINES ET AUTRES HETEROCYCLES AZOTES DERIVES D'AZINE-CARBOXALDEHYDES

Maury, Georges,Meziane, Driss,Srairi, Driss,Paugan, Jean-Paul,Paugam, Renee

, p. 153 - 162 (2007/10/02)

α-(N)-azine-carboxaldehydes are convenient precursors of 1,2,3-triazoloazines.Through oxidative cyclisation of the corresponding hydrazones we have prepared the new 1,2,3-triazolopyridazine and 1,2,3-triazolopyrazine.Unlike the other azaindolizines these compounds are degraded by electrophiles. attempts to prepare imidazopyrimidine or derivatives have been carried out either from 4-aminomethylpyrimidine or from ethyl 2-(4-pyrimidinyl)propionate.

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