Awesome Chemistry Experiments For 16710-11-5

I hope my short article helps more people learn about this compound(4-Methyl-6-(methylthio)pyrimidin-2-ol)Safety of 4-Methyl-6-(methylthio)pyrimidin-2-ol. Apart from the compound(16710-11-5), you can read my other articles to know other related compounds.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 16710-11-5, is researched, SMILESS is CSC1=NC(O)=NC(C)=C1, Molecular C6H8N2OSJournal, Article, Journal of Organic Chemistry called Pyrimidine nucleosides. I. Synthesis of 6-methylcytidine, 6-methyluridine, and related 6-methylpyrimidine nucleosides, Author is Winkley, Michael W.; Robins, Roland K., the main research direction is pyrimidine nucleosides; nucleosides pyrimidine; cytosines; cytidines; uridines; uracils; ribofuranosyls; methylpyrimidine nucleosides.Safety of 4-Methyl-6-(methylthio)pyrimidin-2-ol.

Synthesis of 6-methylprimidine nucleosides was realized. 6-Methylcytidine (I) and 6-methyl-2′-deoxycytidine were prepared by direct utilization of 6-methylcytosine (II) via silylation and subsequent treatment with the appropriate per-O-acetylglycosyl halide in MeCN. Conversion of I into 6-methyluridine was achieved in 65% yield. This direct glycosylation procedure applied to 6-methyluracil gave 6-methyl-3-(β-D-ribofuranosyl)uracil as the major product. Utilization of this general method resulted in preparation of 5,6-dimethyluridine. A new route to the synthesis of II is reported. 31 references.

I hope my short article helps more people learn about this compound(4-Methyl-6-(methylthio)pyrimidin-2-ol)Safety of 4-Methyl-6-(methylthio)pyrimidin-2-ol. Apart from the compound(16710-11-5), you can read my other articles to know other related compounds.

Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem