Some low molecular weight alcohols of industrial importance are produced by the addition of water to alkenes. 7748-36-9, formula is C3H6O2, Ethanol, isopropanol, 2-butanol, and tert-butanol are produced by this general method. Two implementations are employed, the direct and indirect methods. Safety of Oxetan-3-ol
Wu, Hongxiang;Guo, Weijie;Daniel, Stelck;Li, Yue;Liu, Chao;Zeng, Zhuo research published 《 Fluoride-Catalyzed Esterification of Amides》, the research content is summarized as follows. A new method was designed for fluoride-catalyzed activation of secondary and primary amides. This method was enabled the synthesis of esters I [R1 = Ph, 2-thienyl, cyclohexyl, etc.; R2 = n-hexyl, CH2-2-furyl, 3-oxetanyl, etc.] from a wide range of amides using fluoride as a catalyst and alc. as a nucleophiles. This method was showing high functional group tolerance and notably it requires only a slight excess of the alc. nucleophile, which was a rare case in transition-metal-free amide transformations. This approach might provide a new understanding for further studies on esterification of amides and was expected to stimulate the development of alternative methods for direct functionalization of amides.
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., Safety of Oxetan-3-ol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts