Trans-4-(4-chlorophenyl)-1-acetylcyclohexane, with the CAS number 91161-85-2, is an organic compound characterized by its cyclohexane ring substituted with both a chlorophenyl group and an acetyl group. The "trans" configuration indicates that the substituents are positioned on opposite sides of the cyclohexane ring, which influences its three-dimensional shape and reactivity. This compound typically exhibits moderate solubility in organic solvents due to its hydrophobic cyclohexane structure and the presence of polar functional groups. The chlorophenyl moiety contributes to its potential biological activity, as halogenated aromatic compounds often exhibit unique pharmacological properties. Additionally, the acetyl group can participate in various chemical reactions, such as acylation and esterification. The compound's stability and reactivity can be influenced by factors such as temperature and the presence of other reactive species. Overall, trans-4-(4-chlorophenyl)-1-acetylcyclohexane is of interest in both synthetic organic chemistry and potential applications in pharmaceuticals or agrochemicals.

trans-4-(4-chlorophenyl)-1-acetylcyclohexane

91161-85-2: Trans-4-(4-chlorophenyl)-1-acetylcyclohexane, with the CAS number 91161-85-2, is an organic compound characterized by its cyclohexane ring substituted with both a chlorophenyl group and an acetyl group. The "trans" configuration indicates that the substituents are positioned on opposite sides of the cyclohexane ring, which influences its three-dimensional shape and reactivity. This compound typically exhibits moderate solubility in organic solvents due to its hydrophobic cyclohexane structure and the presence of polar functional groups. The chlorophenyl moiety contributes to its potential biological activity, as halogenated aromatic compounds often exhibit unique pharmacological properties. Additionally, the acetyl group can participate in various chemical reactions, such as acylation and esterification. The compound's stability and reactivity can be influenced by factors such as temperature and the presence of other reactive species. Overall, trans-4-(4-chlorophenyl)-1-acetylcyclohexane is of interest in both synthetic organic chemistry and potential applications in pharmaceuticals or agrochemicals.

CAS 91161-85-2

trans-4-(4-chlorophenyl)-1-acetylcyclohexane

Atovaquone Impurity 1

Ref: 4Z-A-2711

trans-4-(4-Chlorophenyl)-1-acetylcyclohexane

Ref: TR-C375460

Atovaquone Impurity 1

Ref: ST-EA-CP-A33010