1004-65-5 Usage
Description
3-Methyl-1,2,4-triazolo[4,3-a]pyridine, also known as 3-Methyl-[1,2,4]triazolo[4,3-a]pyridine, is a chemical compound that belongs to the family of pyridines and derivatives. It is characterized by its aromatic, heterocyclic nature, which is common among chemicals in this category. While specific details about its properties, such as toxicity or potential risks, may vary, it is essential to handle this compound with care to ensure safety and prevent health hazards. Further scientific research is often required to determine its precise chemical behavior, boiling point, melting point, and density.
Uses
Used in Scientific Research:
3-Methyl-1,2,4-triazolo[4,3-a]pyridine is used as a research chemical for various scientific studies. Its unique structure and properties make it a valuable compound for exploring new chemical reactions and understanding its potential applications in different fields.
Used in Industrial Applications:
In the industrial sector, 3-Methyl-1,2,4-triazolo[4,3-a]pyridine is employed as a specialty chemical in the development of new materials and products. Its heterocyclic nature and aromatic characteristics contribute to its versatility in various chemical processes and formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 1004-65-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1004-65:
(6*1)+(5*0)+(4*0)+(3*4)+(2*6)+(1*5)=35
35 % 10 = 5
So 1004-65-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c1-6-8-9-7-4-2-3-5-10(6)7/h2-5H,1H3
1004-65-5Relevant articles and documents
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Yakhontov et al.
, (1972)
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Metal free [4+1] and [5+1] annulation reactions to prepare heterocycles using DMF and its derivatives as one-carbon source
Liu, Lingfeng,Qiao, Chunhua,Shen, Bei,Xu, Yiwen
, (2020/04/01)
1,2,4-Triazolo[3,4-a]pyridines and related heterocycles and substituted triazines were commonly discovered scaffolds in a variety of pharmaceutical and agrochemical agents. Herein, we report a highly efficient and practical method using DMF and its derivative for the [4+1] and [5+1] annulation reactions to prepare these heterocycles. This metal free reaction takes advantages of shelf stable DMF as solvent and carbon donor, imidazole chloride as a catalyst, the mild reaction condition tolerates a broad substrate range and substitutes. The prepared 3-unsubstituted 1,2,4-triazolo[3,4-a]pyridine and derivatives allow further introduction of a variety of functional group1 at 3-position.
Reactions of acylglycines with heteroarylhydrazines
Music, Irena,Vercek, Bojan
, p. 321 - 324 (2007/10/03)
Reactions of N-acylglycines with heteroarylhydrazines leading to acylamino substituted fused 1,2,4-triazoles and N-{2-[2-(heteroaryl)hydrazino]-2-oxoethyl} benzamides have been investigated.
