144105-17-9 Usage
Description
[1,2,4]Triazolo[1,5-c]pyrimidine-5,7-diamine(9CI) is a heterocyclic organic compound with the molecular formula C6H7N7. It belongs to the class of triazolopyrimidine compounds and features a triazolo[1,5-c]pyrimidine ring system. [1,2,4]Triazolo[1,5-c]pyrimidine-5,7-diamine(9CI) has been studied for its potential pharmacological properties, including antitumor and antiviral activities, making it a significant subject for research and development in medicinal chemistry and drug discovery.
Uses
Used in Pharmaceutical Industry:
[1,2,4]Triazolo[1,5-c]pyrimidine-5,7-diamine(9CI) is used as a key intermediate compound for the synthesis of various pharmaceuticals. Its unique structure and pharmacological properties contribute to the development of new drugs with potential applications in treating different diseases.
Used in Agrochemical Industry:
In the agrochemical industry, [1,2,4]Triazolo[1,5-c]pyrimidine-5,7-diamine(9CI) is utilized as a building block for the creation of novel agrochemicals. Its incorporation into these products can lead to the development of more effective and targeted solutions for agricultural challenges, such as pest control and crop protection.
Used in Medicinal Chemistry Research:
[1,2,4]Triazolo[1,5-c]pyrimidine-5,7-diamine(9CI) serves as an important research compound in the field of medicinal chemistry. Its antitumor and antiviral activities make it a promising candidate for further investigation into its potential therapeutic applications, ultimately contributing to the advancement of drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 144105-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,0 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144105-17:
(8*1)+(7*4)+(6*4)+(5*1)+(4*0)+(3*5)+(2*1)+(1*7)=89
89 % 10 = 9
So 144105-17-9 is a valid CAS Registry Number.
144105-17-9Relevant articles and documents
SOME NUCLEOPHILIC SUBSTITUTION REACTIONS OF s-TRIAZOLOPYRIMIDINES
Dianova, L. N.,Koksharova, T.G.,Volkova, N. V.
, p. 321 - 323 (1992)
Nucleophilic substitution of 5-methylthio- and 5-cyanomethylthio-7-amino-s-triazolopyrimidines has been carried out using sodium hydroxide, ammonia, hydrazine hydrate, and four amines.The cyanomethyl group is particularly reactive under these condi
