In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 7748-36-9, formula is C3H6O2, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Application In Synthesis of 7748-36-9
Baum, Kurt;Berkowitz, Phillip T.;Grakauskas, Vytautas;Archibald, Thomas G. research published 《 Synthesis of electron-deficient oxetanes. 3-Azidooxetane, 3-nitrooxetane, and 3,3-dinitrooxetane》, the research content is summarized as follows. Oxetane I (R = OH, R1 = H) was prepared by addition of HOAc to epichlorohydrin, protection of the resulting alc. as an acetal, hydrolysis, ring closure, and removal of the protecting group. I (R = N3, R1 = H) was prepared from I (R = 4-MeC6H4SO3, R1 = H) and NaN3. Reduction of the azide with Ph3P or H gave I (R = NH2, R1 = H), and oxidation of the amine with 3-ClC6H4C(O)OOH gave I (R = NO2, R1 = H). Oxidative nitration or reaction with C(NO2)4 gave I (R = R1 = NO2). I (R = N3, R1 = H; R = R1 = NO2) were polymerized with Lewis acids.
Application In Synthesis of 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., 7748-36-9.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts