674287-63-9 Usage
Uses
Used in Pharmaceutical Industry:
5-BROMO-1H-1,2,4-TRIAZOLE-3-CARBOXYLIC ACID is used as a starting material or intermediate for the synthesis of pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, 5-BROMO-1H-1,2,4-TRIAZOLE-3-CARBOXYLIC ACID is used as a building block for the creation of various chemical products. Its ability to participate in different types of chemical reactions makes it a valuable component in the synthesis of a wide range of compounds.
Used in Agricultural Industry:
5-BROMO-1H-1,2,4-TRIAZOLE-3-CARBOXYLIC ACID is used as a precursor in the development of agrochemicals, such as pesticides and herbicides. Its reactivity and structural properties contribute to the creation of effective compounds for crop protection and management.
Used in Research and Development:
5-BROMO-1H-1,2,4-TRIAZOLE-3-CARBOXYLIC ACID is employed as a research compound in academic and industrial laboratories. Its unique properties make it an interesting subject for studying chemical reactions, synthesis pathways, and potential applications in various fields.
Used in Material Science:
In the field of material science, 5-BROMO-1H-1,2,4-TRIAZOLE-3-CARBOXYLIC ACID may be used as a component in the development of new materials with specific properties. Its reactivity and structural characteristics can contribute to the creation of innovative materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 674287-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,4,2,8 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 674287-63:
(8*6)+(7*7)+(6*4)+(5*2)+(4*8)+(3*7)+(2*6)+(1*3)=199
199 % 10 = 9
So 674287-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H2BrN3O2/c4-3-5-1(2(8)9)6-7-3/h(H,8,9)(H,5,6,7)
674287-63-9Relevant 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.
