CAS 100633-61-2

Trans-4-fluorophenyl 4-ethylcyclohexanecarboxylate is an organic compound characterized by its ester functional group, which is formed from the reaction of a carboxylic acid and an alcohol. This compound features a trans configuration, indicating that the substituents on the cyclohexane ring are positioned opposite each other, which can influence its physical and chemical properties, such as boiling point and solubility. The presence of the fluorine atom in the phenyl group can enhance the compound's lipophilicity and potentially affect its reactivity and interaction with biological systems. Its structure suggests it may exhibit interesting properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals. Additionally, the compound's molecular weight, density, and solubility in various solvents would be important for applications in synthesis and formulation. Safety data, including toxicity and handling precautions, should be consulted when working with this substance, as with any chemical compound. Overall, trans-4-fluorophenyl 4-ethylcyclohexanecarboxylate represents a unique structure with potential applications in various fields of chemistry.