Category: alcohols-buliding-blocks, In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl functional group (−OH) bound to a saturated carbon atom. 7748-36-9, name is Oxetan-3-ol, An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula CnH2n+1OH.
Yang, Wen;Wang, Zhaobin;Sun, Jianwei research published 《 Enantioselective Oxetane Ring Opening with Chloride: Unusual Use of Wet Molecular Sieves for the Controlled Release of HCl》, the research content is summarized as follows. In the presence of a nonracemic spirobiindanephosphoric acid, 3-substituted oxetanes underwent enantioselective ring opening and desymmetrization with chloride generated in situ from trimethoxychlorosilane and water in the presence of 5Å mol. sieves in benzene to yield nonracemic chloropropanols such as (R)-HOCH2CHRCH2Cl [R = Ph, 4-MeC6H4, 2-MeOC6H4, 3-BrC6H4, 3-F3CC6H4, 4-F3CC6H4, 2-naphthyl, 2-benzofuranyl, (E)-PhCH:CH, PhCH2, PhCH2O] as highly functionalized three-carbon building blocks. The excellent enantiocontrol is enabled not only by the use of the new spirobiindanephosphoric acid catalyst, but also by the unusual use of wet mol. sieves for the controlled release of HCl.
7748-36-9, Oxetan-3-ol is a useful research compound. Its molecular formula is C3H6O2 and its molecular weight is 74.08 g/mol. The purity is usually 95%.
Oxetan-3-ol is a synthetic hydroxy compound with the chemical formula C6H12O3. It is an organic solvent that can be used in reactions involving vinyl alcohol and oxetane, such as ring-opening polymerization and cationic polymerization. Oxetan-3-ol has also been shown to react with ethyl bromoacetate to form the corresponding oxetane, which can be used as a bioisostere for chloropropane, a potential replacement for chlorofluorocarbons., Category: alcohols-buliding-blocks
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts