Extended knowledge of 1194-22-5

This compound(6-Hydroxy-2-methylpyrimidin-4(3H)-one)Safety of 6-Hydroxy-2-methylpyrimidin-4(3H)-one was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Experimental therapy of stomach ulcers in rats》. Authors are Akimov, A. A.; Pazarev, N. V..The article about the compound:6-Hydroxy-2-methylpyrimidin-4(3H)-onecas:1194-22-5,SMILESS:CC1=NC(=CC(N1)=O)O).Safety of 6-Hydroxy-2-methylpyrimidin-4(3H)-one. Through the article, more information about this compound (cas:1194-22-5) is conveyed.

Gastric ulcers were induced in rats by repeated administration of caffeine by a gastric sonde. Animals were then treated with 4-methyluracil (I), dihydrouracil, dihydro-4-methyluracil, 5-hydroxy-4-methyluracil, thymine, 4,6-dihydroxypyrimidine (II), 2-methyl-4,6-dihydroxypyrimidine (III), cytosine (IV), 4-amino-6-hydroxypyrimidine, or 2-amino-6-oxy-4-methylpyrimidine (all compounds given by gastric sonde, 50 mg./kg.). A 42-72% reduction of ulcers followed the treatment of animals with I, II, III, and IV; with all other compounds the effect was not significant. Combined treatment of rats with I and III, or I and IV was most effective. Higher doses of all compounds tested had a smaller therapeutic effect. Pyrimidines apparently stimulate regenerative processes and thus complement the effect of other therapeutics in the treatment of gastric ulcers.

This compound(6-Hydroxy-2-methylpyrimidin-4(3H)-one)Safety of 6-Hydroxy-2-methylpyrimidin-4(3H)-one was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem