21733-00-6 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 3-nitro-1H-1,2,4-triazole-5-carboxylate is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its reactivity and structural properties make it a valuable component in the creation of new drugs, particularly those targeting specific biological pathways or conditions.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 3-nitro-1H-1,2,4-triazole-5-carboxylate is employed as a precursor in the development of pesticides. Its chemical properties allow for the formulation of effective pest control agents, contributing to agricultural productivity and crop protection.
Used in Energetic Materials:
Methyl 3-nitro-1H-1,2,4-triazole-5-carboxylate is used as a critical component in the production of energetic materials due to its explosive properties. This application is crucial in various fields such as mining, construction, and defense, where controlled explosions are necessary for operations.
Safety and Handling:
Given its explosive nature, Methyl 3-nitro-1H-1,2,4-triazole-5-carboxylate requires careful and controlled use in laboratory and industrial settings. Special safety measures and handling protocols must be adhered to in order to mitigate risks associated with its reactivity and potential for explosion.
Check Digit Verification of cas no
The CAS Registry Mumber 21733-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,3 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21733-00:
(7*2)+(6*1)+(5*7)+(4*3)+(3*3)+(2*0)+(1*0)=76
76 % 10 = 6
So 21733-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N4O4/c1-12-3(9)2-5-4(7-6-2)8(10)11/h1H3,(H,5,6,7)
21733-00-6Relevant academic research and scientific papers
Chemoenzymatic method of 1,2,4-triazole nucleoside synthesis: Possibilities and limitations
Konstantinova,Chudinov,Fateev,Matveev,Zhurilo,Shvets,Miroshnikov
, p. 53 - 71 (2013/04/10)
Possibilities and limitations of chemoenzymatic synthesis of novel structural analogues of an antiviral preparation of Ribavirin (1-β-D-ribofuranosyl-1,2,4-triazole-3-carboxamide) were established. A synthesis of various amides of 1H-1,2,4-triazole-3-carboxylic acid and its 5-substituted analogues - potential substrates of purine nucleoside phosphorylase - has been described. Comparative efficiency of preparation methods of these amides, as well as the methods of introduction of functional groups to the C5 position of heterocyclic system, were investigated. Novel analogues of Ribavirin containing various substitutes in the carboxamide group were synthesized. A biotechnological method was developed for the preparation of 1-β-D-ribofuranozyl-1,2,4-triazole-3-carbonitryl, an intermediate in the synthesis of Viramidine, the modern analogue of Ribavirin.
