4999-42-2 Usage
Description
7-methyl-[1,2,4]triazolo[1,5-a]pyridine is a heterocyclic chemical compound with the molecular formula C7H7N3. It features a triazolopyridine ring system and a methyl group at the 7-position, which contributes to its unique structure and potential pharmacological properties.
Uses
Used in Pharmaceutical Research and Development:
7-methyl-[1,2,4]triazolo[1,5-a]pyridine is utilized as a key intermediate in the synthesis of potential drug candidates. Its unique structure allows for the development of new compounds with therapeutic applications.
Used in Materials Science:
Although not explicitly mentioned in the provided materials, the compound's heterocyclic nature suggests it may have potential uses in materials science, possibly for the development of new materials with specific properties.
Used in Agrochemicals:
Similarly, while not detailed in the materials, the compound's structure may also lend itself to applications in agrochemicals, potentially for the creation of new pesticides or other agricultural chemicals.
The specific properties and potential applications of 7-methyl-[1,2,4]triazolo[1,5-a]pyridine are subject to ongoing research and exploration, indicating that its uses may expand as more is learned about its characteristics and capabilities.
Check Digit Verification of cas no
The CAS Registry Mumber 4999-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4999-42:
(6*4)+(5*9)+(4*9)+(3*9)+(2*4)+(1*2)=142
142 % 10 = 2
So 4999-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c1-6-2-3-10-7(4-6)8-5-9-10/h2-5H,1H3
4999-42-2Relevant articles and documents
New method for the general synthesis of [1,2,4]triazolo[1,5-a]pyridines
Huntsman, Elliott,Balsells, Jaume
, p. 3761 - 3765 (2007/10/03)
[1,2,4]Triazolo[1,5-a]pyridines without substituants on the 2-position have been prepared from 2-aminopyridines by cyclization of N-(pyrid-2-yl) formamidoximes with trifluoroacetic anhydride. Triazoles substituted at any position on the pyridine ring may be prepared in good yields and under mild reaction conditions. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.
