Wang, Zhaobin team published research in Angewandte Chemie, International Edition in 2013 | 7748-36-9

Related Products 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.

Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 7748-36-9, formula is C3H6O2, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , Related Products of 7748-36-9

Wang, Zhaobin;Chen, Zhilong;Sun, Jianwei research published 《 Catalytic Enantioselective Intermolecular Desymmetrization of 3-Substituted Oxetanes》, the research content is summarized as follows. Under optimized reaction conditions, the synthesis of the target compounds was achieved using (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-di(9-phenanthrenyl)diindeno[7,1-de:1′,7′-fg][1,3,2]dioxaphosphocin 5-oxide (chiral cyclic phosphate) as a catalyst. A stereoselective ring opening reaction of 3-(phenyl)oxetane (I) with 2(3H)-benzothiazolethione [thiol, 2-(mercapto)benzothiazole] gave a chiral mercapto alc. (II).

Related Products 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