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. , Computed Properties of 7748-36-9
Helmkamp, George K.;Clark, Ronald D.;Koskinen, James R. research published 《 Quaternization of aziridines. Evidence for the monomeric state of products》, the research content is summarized as follows. cis-(I) or trans-1,2,3-Trimethylaziridine (II), cis- (III) or trans-ethyl-2,3-dimethylaziridine (IV) when treated with MeI afforded a solid which was found to decompose readily. It could not be assumed that the materials from I-IV were monomeric species. When the MeI salts of I-IV were treated with Ag 2,4,6-trinitrobenzenesulfonate, stable salts were obtained. Attempts to obtain mol. weights indicated the compounds appeared to be dimeric when MeCN and Ph2 was used but in alc. the results were equivocal. Optically active 1,2,3-trimethylaziridine (V) formed a MeI salt (VI) which was optically active, and its structure was considered to be monomeric. Further confirmation was obtained by treatment of VI with excess NH3 to give an optically active compound, whereas with NHMe2, meso-2,3-bis(dimethylamino)butane was obtained. The reactions with NH3 and NHMe2 were followed polarimetrically. The fact that the alkylation product of an aziridine reacted readily with a nucleophile verified the conclusion that the three-membered ring remained intact and retention of optical activity excluded racemization as a principal feature of the process.
Computed Properties 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