Nikolaev, Andrei team published research in Synthesis in 2016 | 16545-68-9

16545-68-9, Cyclopropanol is a cyclopropane in which a hydrogen atom is replaced by a hydroxy group. It is a member of cyclopropanes and an aliphatic alcohol.
Cyclopropanol is a useful research compound. Its molecular formula is C3H6O and its molecular weight is 58.08 g/mol. The purity is usually 95%.
Cyclopropanol is a cyclic organic compound that is synthesized from sodium hydroxide solution, nitrogen atoms, and carbonyl groups. Cyclopropanol has shown inhibitory effects on inflammatory bowel disease in rats. This drug also inhibits the production of hydrogen chloride and hydrochloric acid in the stomach, which can lead to ulcers. Cyclopropanol has been found to be effective against bowel diseases such as Crohn’s disease and ulcerative colitis. This drug has been shown to have strong antioxidant properties, which may be due to its ability to reduce hydroxyl radicals., COA of Formula: C3H6O

In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 16545-68-9, formula is C3H6O, 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. COA of Formula: C3H6O

Nikolaev, Andrei;Orellana, Arturo research published 《 Transition-Metal-Catalyzed C-C and C-X Bond-Forming Reactions Using Cyclopropanols》, the research content is summarized as follows. A review. Due to their high strain, unique bonding and relative ease of ring-cleavage, and because they are readily accessible, cyclopropanols were employed in an increasing number of transition-metal-catalyzed C-C and C-X (X = heteroatom) bond-forming reactions. The authors review the recent literature and organize all the methods developed along mechanistic lines. C-C bond formation via catalytic generation and coupling of cyclopropanol-derived homoenolates. C-N bond formation via catalytic generation and coupling of cyclopropanol-derived homoenolates. C-C bond formation via stoichiometric generation and coupling of cyclopropanol-derived homoenolates. Ring expansion of cyclopropanols to cyclobutanones via transition-metal-catalyzed wagner-meerwein shift. Transition-metal-catalyzed rearrangement of cyclopropanols to cyclopentenones and cyclohexenones. Synthesis of medium-size rings via multicomponent reactions involving cyclopropanols. C-C and C-X bond formation via free-radical fragmentation of cyclopropanols.

16545-68-9, Cyclopropanol is a cyclopropane in which a hydrogen atom is replaced by a hydroxy group. It is a member of cyclopropanes and an aliphatic alcohol.
Cyclopropanol is a useful research compound. Its molecular formula is C3H6O and its molecular weight is 58.08 g/mol. The purity is usually 95%.
Cyclopropanol is a cyclic organic compound that is synthesized from sodium hydroxide solution, nitrogen atoms, and carbonyl groups. Cyclopropanol has shown inhibitory effects on inflammatory bowel disease in rats. This drug also inhibits the production of hydrogen chloride and hydrochloric acid in the stomach, which can lead to ulcers. Cyclopropanol has been found to be effective against bowel diseases such as Crohn’s disease and ulcerative colitis. This drug has been shown to have strong antioxidant properties, which may be due to its ability to reduce hydroxyl radicals., COA of Formula: C3H6O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts