In 1968,Journal of Pharmaceutical Sciences included an article by Venturella, Vincent S.. Safety of 6-Methoxypyrimidine-2,4(1H,3H)-dione. The article was titled 《Selective acid-catalyzed hydrolyses of methoxysulfanilamidodiazines》. The information in the text is summarized as follows:
The dilute acid hydrolysis of 3-methoxy-6-sulfanilamidopyridazine and several methoxysulfanilamidopyrimidines was studied. Experiments show that in cases where an intermediate 2-pyrimidone is a possible postulation, further hydrolysis usually leads to the formation of sulfanilamide and the corresponding hydroxypyrimidine. A multistage route for the acidic degradation of 3-methoxy-6-sulfanilamidopyridazine, 2,4-dimethoxy-6-sulfanilamidopyrimidine, and 2-methylthio-4-methoxy-6-sulfanilamidopyrimidine is proposed. 26 references. In the experimental materials used by the author, we found 6-Methoxypyrimidine-2,4(1H,3H)-dione(cas: 29458-38-6Safety of 6-Methoxypyrimidine-2,4(1H,3H)-dione)
6-Methoxypyrimidine-2,4(1H,3H)-dione(cas: 29458-38-6) belongs to pyrimidine. Pyrimidine nucleotide derivatives have a wide range of biological applications. For example, pyrimidine derivatives are useful in DNA repair studies involving cancer and epigenetics.Safety of 6-Methoxypyrimidine-2,4(1H,3H)-dione
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia