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
DeRatt, Lindsey G.;Wang, Chao-Yuan;Kuduk, Scott D. research published 《 Tandem Amination/Oxetane Ring Opening toward Benzomorpholines》, the research content is summarized as follows. Herein, a tandem approach that allowed rapid access to the benzomorpholine such as I [R1 = 5-F, 5-Me, 8-Cl, etc.], II [R = Ms, Ts, Ns, etc.; R2 = 8-Cl, 6-MeO, 7-CF3, etc.; R3 = H, Me] scaffold was reported. This operationally simple method allowed for valuable heterocycles to be isolated in moderate to high yields. The overall transformation consisted of an initial C-N coupling, demonstrated using traditional Ullmann or Buchwald-Hartwig conditions, followed by an in situ oxetane ring opening. A range of functionality was tolerated on the aryl ring, and the cyclization exposes a pendant hydroxymethyl substituent, providing opportunities for further functionalization.
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