4931-27-5 Usage
Description
5-methyl-[1,2,4]triazolo[1,5-a]pyridine is a heterocyclic chemical compound belonging to the class of triazolopyridines. It has a molecular formula of C8H7N3 and a molecular weight of 145.16 g/mol. 5-methyl-[1,2,4]triazolo[1,5-a]pyridine is known for its unique structure and reactivity, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
5-methyl-[1,2,4]triazolo[1,5-a]pyridine is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity contribute to the development of potential drug candidates for the treatment of different diseases, including cancer and neurological disorders.
Used in Agrochemical Industry:
In the agrochemical industry, 5-methyl-[1,2,4]triazolo[1,5-a]pyridine is utilized as a key component in the synthesis of agrochemicals. Its properties make it suitable for the development of new compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Medicinal Chemistry Research:
5-methyl-[1,2,4]triazolo[1,5-a]pyridine is also used as an important compound in medicinal chemistry research. Its potential as a bioactive molecule in various biological assays makes it a valuable tool for studying the mechanisms of action and developing new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 4931-27-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4931-27:
(6*4)+(5*9)+(4*3)+(3*1)+(2*2)+(1*7)=95
95 % 10 = 5
So 4931-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c1-6-3-2-4-7-8-5-9-10(6)7/h2-5H,1H3
4931-27-5Relevant 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.
