16545-68-9OC1CC1YOXHCYXIAVIFCZ-UHFFFAOYSA-NCyclopropanol is a cyclopropane in which a hydrogen atom is replaced by a hydroxy group. It is an aliphatic alcohol and a member of cyclopropanes.
16545-68-9DTXSID40167949CHEBI:188444化学性质シクロプロパノールは分子式がC3H6Oで表される有機化合物ですこの分子は三員環構造を持ちその一部に酸素が含まれていることが特徴ですこの特異な環構造によりシクロプロパノールは高いひずみエネルギーを持ち化学的に非常に反応しやすい状態にあります
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Danger
H301 (88.4%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 43 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
説明Cyclopropanols can be readily synthesized via synthetic transformations such as the Kulinkovich cyclopropanation and the Simmons-Smith reaction [1]. Due to the high strains built intrinsically in the three-membered ring, cyclopropanols and their derivatives are highly reactive and can undergo various ring opening/expansion/fragmentation reactions. A significant amount of these ring opening/expansion/fragmentation reactions are catalyzed/promoted by transition metal complexes. In many of these cases, cyclopropanols and their derivatives are considered as the equivalents of homoenolates or β-alkyl radicals.
使用Cyclopropanol is a basic building block.
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