504-17-6, Adding a certain compound to certain chemical reactions, such as: 504-17-6, 4,6-Dihydroxy-2-mercaptopyrimidine, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, 504-17-6, blongs to pyrimidines compound.
General procedure: A mixture of aldehyde (1 mmoL), (thio)barbituric acid(1 mmoL) and verjuice (10 mL) was heated in an oil bath(60 C). After completion of the reaction, as monitored byTLC, using n-hexane:EtOAc (7:3) as the eluent, the reactionmixture was filtered and the precipitated product was washedwith water (3 ¡Á 10 mL) to afford the pure compound.
These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,504-17-6, its application will become more common.
Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of the Iranian Chemical Society; vol. 16; 4; (2019); p. 887 – 897;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia