1313739-06-8 Usage
Description
Ethyl 2-(2-Methyl-[1,2,4]-Triazol-3-yl)-2-oxoacetate is an organic compound characterized by its triazole and ester functional groups. It is a key intermediate in the synthesis of various heterocyclic compounds, particularly azolylquinoxalinones, due to its unique chemical structure and reactivity.
Uses
Used in Pharmaceutical Industry:
Ethyl 2-(2-Methyl-[1,2,4]-Triazol-3-yl)-2-oxoacetate is used as a synthetic intermediate for the preparation of azolylquinoxalinones, which are compounds of interest in the pharmaceutical industry. These azolylquinoxalinones have potential applications as therapeutic agents, particularly in the development of novel drugs targeting various diseases and conditions.
Used in Chemical Research:
In the field of chemical research, Ethyl 2-(2-Methyl-[1,2,4]-Triazol-3-yl)-2-oxoacetate serves as a valuable building block for the synthesis of complex organic molecules. Its unique structure allows for further functionalization and modification, making it a versatile compound for exploring new chemical reactions and developing innovative synthetic routes.
Used in Material Science:
Ethyl 2-(2-Methyl-[1,2,4]-Triazol-3-yl)-2-oxoacetate may also find applications in material science, particularly in the development of new materials with specific properties. The triazole and ester groups present in the molecule can be exploited to create materials with tailored characteristics, such as improved stability, reactivity, or selectivity, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 1313739-06-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,7,3 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1313739-06:
(9*1)+(8*3)+(7*1)+(6*3)+(5*7)+(4*3)+(3*9)+(2*0)+(1*6)=138
138 % 10 = 8
So 1313739-06-8 is a valid CAS Registry Number.
1313739-06-8Relevant articles and documents
Facile synthesis of 2-(2-ethoxy-1,2-dioxoethyl)azoles
Geraschenko, Oleksandr V.,Khodakovskiy, Pavel V.,Shishkin, Oleg V.,Mykhailiuk, Pavel K.,Zaporozhets, Olga A.,Tolmachev, Andrey A.
experimental part, p. 1633 - 1637 (2011/06/25)
C-Acylation of N-substituted imidazoles with ethyl oxalyl chloride in the presence of N,N-diisopropylethylamine as a base afforded 2-(2-ethoxy-1,2- dioxoethyl)imidazoles in 83-95% yield. Application of this synthetic protocol to thiazoles and triazoles le
