Brief introduction of 6-Methylpyrimidine-2,4(1H,3H)-dione

Reference of 626-48-2, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 626-48-2 is helpful to your research.

Reference of 626-48-2, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 626-48-2, Name is 6-Methylpyrimidine-2,4(1H,3H)-dione, SMILES is CC1=CC(NC(N1)=O)=O, belongs to pyrimidines compound. In a article, author is Lyapustin, Daniil N., introduce new discover of the category.

6-Nitro-4,7-dihydroazolo [1,5-a]pyrimidines: an alternative mechanism of formation and studies of alkylation

The mechanism of a multicomponent reaction between aminoazoles, 1-morpholino-2-nitroalkenes, and benzaldehyde was studied in acidic medium. Performing the reaction in acetic acid led to the formation of 6-nitro-5-phenyl-4,5,6,7-tetrahydropyrazolo[1,5-a]-pyrimidines, which subsequently underwent a rearrangement. Reaction conditions were proposed for a multicomponent synthesis with trioxane, and the alkylation reactions of 4,7-dihydroazolo[1,5-a]pyrimidine nitro derivatives were optimized.

Reference of 626-48-2, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 626-48-2 is helpful to your research.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia