2-Benzylcyclohexanone (CAS 946-33-8)

2-Benzylcyclohexanone, referred to as 2-BCH, serves as a valuable organic compound extensively employed across scientific and industrial domains. This unique substance is a derivative of cyclohexanone, distinguished by the attachment of a benzyl group to the 2-position of the cyclohexane ring. At room temperature, 2-Benzylcyclohexanone appears as a colorless liquid exuding a pleasant, fruity aroma. It exhibits good solubility in various organic solvents, including ethanol and ether, and remains stable under standard conditions. Its versatility renders 2-Benzylcyclohexanone a prominent player in scientific research applications. Notably, it finds purpose as a reagent in organic synthesis, facilitates chromatographic separations as a solvent, and participates as a reactant in compound synthesis endeavors. Furthermore, it has proved invaluable in the study of cyclohexanones and related compounds, standing as a reliable model for such chemical investigations. Although the precise mechanism of action of 2-Benzylcyclohexanone remains somewhat enigmatic, it is widely believed that the benzyl group at the 2-position of the cyclohexane ring contributes significantly to its activity. This functional group seemingly enhances the reactivity of the cyclohexanone moiety, enabling the formation of novel compounds and catalyzing diverse reactions.