100589-03-5 Usage
Description
[1,2,4]Triazolo[1,5-a]pyrimidine, 1,7-dihydro-5-methyl-7-phenylis a heterocyclic chemical compound belonging to the triazolopyrimidine family. It features a triazole ring fused to a pyrimidine ring, with a 1,7-dihydro-5-methyl-7-phenylsubstituent attached to the pyrimidine ring. This unique structure endows the compound with distinct properties and potential applications in various fields, particularly in the development of new drugs and as a building block in organic synthesis. Its pharmacological and biological activities have been a subject of interest, making it a promising candidate for further research and development in medicinal chemistry and drug discovery.
Uses
Used in Pharmaceutical Industry:
[1,2,4]Triazolo[1,5-a]pyrimidine, 1,7-dihydro-5-methyl-7-phenylis used as a potential candidate for the development of new drugs due to its unique structural features and pharmacological properties. Its heterocyclic nature and the presence of the 1,7-dihydro-5-methyl-7-phenylsubstituent may contribute to its interaction with specific biological targets, making it a valuable compound for the creation of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, [1,2,4]Triazolo[1,5-a]pyrimidine, 1,7-dihydro-5-methyl-7-phenylserves as a building block for the synthesis of more complex molecules. Its structural features can be exploited to create a variety of compounds with diverse applications, including those in the pharmaceutical, agrochemical, and materials science industries. [1,2,4]Triazolo[1,5-a]pyrimidine, 1,7-dihydro-5-methyl-7-phenyl-'s potential as a synthetic intermediate highlights its importance in the development of new chemical entities with specific functionalities and properties.
Used in Medicinal Chemistry Research:
[1,2,4]Triazolo[1,5-a]pyrimidine, 1,7-dihydro-5-methyl-7-phenylis utilized in medicinal chemistry research to explore its potential pharmacological and biological activities. [1,2,4]Triazolo[1,5-a]pyrimidine, 1,7-dihydro-5-methyl-7-phenyl-'s unique structure allows researchers to investigate its interactions with various biological targets, which could lead to the discovery of new therapeutic agents or a better understanding of existing drug mechanisms. This research can contribute to the advancement of drug discovery and the development of more effective treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 100589-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,8 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100589-03:
(8*1)+(7*0)+(6*0)+(5*5)+(4*8)+(3*9)+(2*0)+(1*3)=95
95 % 10 = 5
So 100589-03-5 is a valid CAS Registry Number.
100589-03-5Relevant articles and documents
CHEMICAL CONVERSIONS OF 5,7-DISUBSTITUTED DIHYDRO-1,2,4-TRIAZOLOPYRIMIDINES
Desenko, S. M.,Orlov, V. D.,Lipson, V. V.
, p. 1362 - 1366 (1990)
Hydrolysis, oxidation, reduction, alkylation, and nitrosation of aromatic-substituted dihydro-1,2,4-triazolopyrimidines have been studied.
