769-97-1 Usage
General Description
4-Pyrimidinecarboxamide, 1,2,3,6-tetrahydro-2,6-dioxo- is a chemical compound that belongs to the class of pyrimidine carboxamides. It is a crystalline solid with the molecular formula C6H6N4O2 and a molecular weight of 166.14 g/mol. 4-PyriMidinecarboxaMide, 1,2,3,6-tetrahydro-2,6-dioxo- is used in the synthesis of pharmaceuticals and agrochemicals. It is also known for its potential anticonvulsant and neuroprotective properties, making it a subject of interest in the field of medicinal chemistry. Additionally, it can be utilized as a building block in the production of various heterocyclic compounds.
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 articles and documents
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.