Adding a certain compound to certain chemical reactions, such as: 65-71-4, 5-Methylpyrimidine-2,4(1H,3H)-dione, 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, Application In Synthesis of 5-Methylpyrimidine-2,4(1H,3H)-dione, blongs to pyrimidines compound. Application In Synthesis of 5-Methylpyrimidine-2,4(1H,3H)-dione
Thymine (T) was purchased from Sigma Aldrich and K2S2O8from SRL. All the solutions were prepared with water purified by Cascada Lab Water Systems and of resistivity 18.2M Omega cm. The sulfate radicals were produced by the UV-photolysis of peroxide asreported elsewhere [39]. The solution containing T (10-4 M) and K2S2O8 (10-3 M) was subjected to UV irradiation at a wavelength of 254 nm for about 2 min. The solution was then directly subjected to UPLC-ESI-CID analysis.
At the same time, in my other blogs, there are other synthetic methods of this type of compound,65-71-4, 5-Methylpyrimidine-2,4(1H,3H)-dione, and friends who are interested can also refer to it.
Reference:
Article; Chandran, Jisha; Vishnu; Aravind, Usha K.; Aravindakumar; International Journal of Mass Spectrometry; vol. 443; (2019); p. 53 – 60;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia