34550-62-4 Usage
Uses
Used in Pharmaceutical Industry:
3H-[1,2,3]Triazolo[4,5-c]pyridin-4-amine is used as a kinase inhibitor for its potential role in the treatment of various diseases. Its ability to inhibit specific kinases may contribute to the regulation of cellular processes and pathways, offering therapeutic benefits in conditions where kinase activity is dysregulated.
Used in Medicinal Chemistry Research:
3H-[1,2,3]Triazolo[4,5-c]pyridin-4-amine serves as an interesting target for medicinal chemistry research due to its unique structure and potential biological activities. Researchers are exploring its mechanism of action, pharmacological properties, and possible applications in drug development to harness its therapeutic potential.
Further studies are necessary to fully understand the mechanism of action of 3H-[1,2,3]Triazolo[4,5-c]pyridin-4-amine and to evaluate its safety and efficacy in preclinical and clinical settings. This will help in determining its suitability as a therapeutic agent and its potential impact on the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 34550-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,5 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34550-62:
(7*3)+(6*4)+(5*5)+(4*5)+(3*0)+(2*6)+(1*2)=104
104 % 10 = 4
So 34550-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N5/c6-5-4-3(1-2-7-5)8-10-9-4/h1-2H,(H2,6,7)(H,8,9,10)
34550-62-4Relevant academic research and scientific papers
Yutilov,Smolyar
, p. 1526 - 1527 (2004)
Treatment of 3,4-bis(formylamino)pyridine with a mixture of concentrated nitric and sulfuric acids unexpectedly afforded 4-nitro-1,2,3-triazolo[4,5-c] pyridine 2-oxide. Reduction of the latter with iron in acetic acid gave previously known 4-amino-1,2,3-triazolo[4,5-c]pyridine.
Cyclization of substituted 3,4-diaminopyridines into 1H-[1,2,3]triazolo[4, 5-c]pyridine 2-oxide derivatives during the nitration process
Smolyar,Vasilechko
experimental part, p. 1219 - 1222 (2011/01/04)
The nitration of pyridine-3,4-diamine, its N,N'-diacetyl derivative, and N4-alkylpyridine-3,4-di- amines with excess nitric acid in concentrated sulfuric acid at 60°C was accompanied by cyclization with formation of the corresponding 1-substitu
