Yates, Peter team published research in Tetrahedron Letters in 1965 | 7748-36-9

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.

Application In Synthesis of 7748-36-9, 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.

Yates, Peter;Szabo, Arthur G. research published 《 Photochemical synthesis of 3-oxetanols》, the research content is summarized as follows. Irradiation of 1% solution of RCOCH2OCH2R’ (I, R = Ph, R’ = H) (II) in C6H6 (N atm.) 12 hrs. with a 450-w., H2O-cooled, high pressure Hg lamp yielded 29% 3-phenyl-3-oxetanol (III, R = Ph, R’ = H) (IV), m. 55-6° The N.M.R. signal at 6.28 ppm. was absent after treatment with D2O. Treatment of 3-oxetanone with PhMgBr followed by decomposition with aqueous NH4Cl also yielded IV. Identification of BzMe and H2CO among the products of the photochem. reaction showed that the synthesis of IV was accompanied by a Norrish type II cleavage of the alkoxy ketone (Srinivasan, CA 57, 7091i). Similar irradiation of I (R = Ph, R’ = Me) yielded 34% III (R = Ph, R’ = Me) (V), b0.5 75-80°, n25D 1.5392; V consisted largely or entirely of a single diastereoisomeric form. Irradiation of I (R = tert-Bu, R’ = H) yielded only 5% III (R = tert-Bu, R’ = H), m. 118-19.5° (after sublimation), indicating that the reaction is not restricted to aromatic ketones.

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