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[1,2,4]Triazolo[4,3-a]pyrazine, 97%|194019|274-82-8

[1,2,4]Triazolo[4,3-a]pyrazine, 97%

Cat. No JK194019_100_MG
J&K Chemical

Product Information

Product Name
1,2,4Triazolo4,3-apyrazine, 97%
Brand Name
J&K
Product Number
194019
CAS
274-82-8
Molecular Formula
C5H4N4
Molecular Weight
120.11
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
249778
IUPAC Name
1,2,4triazolo4,3-apyrazine
InChI Key
NVSPJDGXKBDYIZ-UHFFFAOYSA-N
SMILES
C1=CN2C=NN=C2C=N1

Safety Information

Signal Word
Danger
Hazard Statement
H302
H312
H316
H332
H335
H372
Precautionary Statement
P264
P270
P330
P501
P280
P321
P261
P271
P319
P405
P260
P301+P317
P302+P352
P362+P364
P332+P317
P304+P340
P403+P233

References Data Source From Pubchem

Crystallographic Fragment Screen of Coxsackievirus A16 2A Protease identifies new opportunities for the development of broad-spectrum anti-enterovirals
Publication Name: bioRxiv : the preprint server for biology
Publication Date: 2024-04-29
DOI: 10.1101/2024.04.29.591684

Focused small molecule library of 5,6,7,8-tetrahydro[1,2,4]triazolo-[4,3-a]pyrazines: a brick for the house of medicinal chemistry
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2023-07
DOI: 10.1007/s10593-023-03213-y

Synthesis of Novel 1-(1,5-Diaryl-1,10b-Dihydropyrrolo- [1,2-A][1,2,4]Triazolo[3,4-C]Pyrazin-3-Yl)Ethanones Via 1,3-Dipolar Cycloaddition of Nitrilimine
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2020-01
DOI: 10.1007/s10593-020-02626-3

Facile one-pot synthesis of N-fused 1,2,4-triazoles via oxidative cyclization using manganese dioxide
Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2018-12
DOI: 10.1007/s10593-019-02400-0

The novel BET bromodomain inhibitor BI 894999 represses super-enhancer-associated transcription and synergizes with CDK9 inhibition in AML
Publication Name: Oncogene
Publication Date: 2018-03-01
DOI: 10.1038/s41388-018-0150-2

[1,2,4]Triazolo[4,3-a]pyrazine, 97%

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