5295-23-8 Usage
Uses
Used in Pharmaceutical Industry:
N-(2H-1,2,4-Triazole-3-yl)acetamide is utilized as a building block or intermediate in the synthesis of pharmaceutical drugs. Its triazole ring structure is known to contribute to the biological activity of various medicinal compounds, making it a valuable component in drug development.
Used in Agrochemical Industry:
In the agrochemical field, N-(2H-1,2,4-Triazole-3-yl)acetamide serves as a key component in the formulation of fungicides. The triazole moiety is recognized for its efficacy in controlling fungal infections, thus playing a crucial role in protecting crops and enhancing agricultural productivity.
Further research and development efforts are directed towards exploring the therapeutic or pesticidal properties of N-(2H-1,2,4-Triazole-3-yl)acetamide, with the aim of expanding its applications and improving its effectiveness in respective industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5295-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5295-23:
(6*5)+(5*2)+(4*9)+(3*5)+(2*2)+(1*3)=98
98 % 10 = 8
So 5295-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4O/c1-3(9)7-4-5-2-6-8-4/h2H,1H3,(H2,5,6,7,8,9)
5295-23-8Relevant academic research and scientific papers
Reaction of arylidene derivatives of Meldrum's acid with 3-amino-1,2,4-triazole
Lipson,Orlov,Desenko,Karnozhitskaya,Shirobokova
, p. 595 - 599 (2007/10/03)
The condensation of arylidene derivatives of Meldrum's acid with 3-amino-1,2,4-triazole in nitrobenzene leads to 4,5,6,7-tetrahydro-1,2,4-triazolo[1,5-a]pyrimidin-5-ones. In DMF the reaction proceeds with the formation of arylsubstituted N-(2H-1,2,4-triazol-3-yl)-3-(2H-1,2,4-triazol-3-ylamino)propionamides. 1999 KluwerAcademic/Plenum Publishers.
