769-97-1 Usage
Uses
Used in Pharmaceutical Synthesis:
4-PyriMidinecarboxaMide, 1,2,3,6-tetrahydro-2,6-dioxois used as a key intermediate in the synthesis of pharmaceuticals. Its unique chemical structure allows it to be incorporated into various drug molecules, enhancing their therapeutic properties and effectiveness.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-PyriMidinecarboxaMide, 1,2,3,6-tetrahydro-2,6-dioxois used as a building block for the development of new agrochemicals. Its incorporation into these compounds can improve their efficacy in controlling pests and diseases, contributing to increased crop yields and better agricultural practices.
Used in Medicinal Chemistry Research:
Due to its potential anticonvulsant and neuroprotective properties, 4-PyriMidinecarboxaMide, 1,2,3,6-tetrahydro-2,6-dioxois a subject of interest in the field of medicinal chemistry. Researchers are exploring its potential applications in the development of new drugs for the treatment of neurological disorders, such as epilepsy and neurodegenerative diseases.
Used in the Production of Heterocyclic Compounds:
4-PyriMidinecarboxaMide, 1,2,3,6-tetrahydro-2,6-dioxocan be utilized as a building block in the production of various heterocyclic compounds. These compounds have a wide range of applications in different industries, including pharmaceuticals, agrochemicals, and materials science. The unique properties of heterocyclic compounds make them valuable in the development of new drugs, agrochemicals, and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 769-97-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 769-97:
(5*7)+(4*6)+(3*9)+(2*9)+(1*7)=111
111 % 10 = 1
So 769-97-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N3O3/c6-4(10)2-1-3(9)8-5(11)7-2/h1H,(H2,6,10)(H2,7,8,9,11)
769-97-1Relevant academic research and scientific papers
Efficient one-pot synthesis of polysubstituted 6-[(1H-1,2,3-Triazol-1-Yl) Methyl]uracils through the "click" protocol
Jansa, Petr,Spacek, Petr,Votruba, Ivan,Brehova, Petra,Dracinsky, Martin,Klepetarova, Blanka,Janeba, Zlatko
experimental part, p. 1121 - 1131 (2012/06/30)
The preparation of several triazolo acyclic nucleosides and triazolo acyclic nucleoside phosphonates is described. The synthetic methodology has been developed as an efficient one-pot Cu(I)-catalyzed azide alkyne Huisgen "click" cycloaddition. A novel Cu(I)-catalyzed decarboxylation reaction of 1-substituted 1H-1,2,3-triazole-4-carboxylic acids at room temperature was observed and used for the preparation of 1-substituted 1H-1,2,3-triazoles. As congeners of TPI (Taiho pharmaceutical inhibitor), the prepared compounds were screened as potential inhibitors of human thymidine phosphorylase, but no inhibitory activity was observed.
