(3-Chloro-5-fluoro-phenyl)-cyclohexyl-methanone, with the CAS number 898769-36-3, is an organic compound characterized by its unique molecular structure, which includes a cyclohexyl group and a phenyl ring substituted with both chlorine and fluorine atoms. This compound typically exhibits properties associated with halogenated aromatic compounds, such as increased lipophilicity and potential biological activity. The presence of the chloro and fluoro substituents can influence its reactivity, stability, and interaction with biological systems, making it of interest in medicinal chemistry and material science. The cyclohexyl moiety contributes to its steric bulk, which may affect its conformational flexibility and overall molecular interactions. Additionally, the compound may exhibit specific solubility characteristics, depending on the solvent used, and could participate in various chemical reactions, including nucleophilic substitutions or electrophilic aromatic substitutions. Overall, this compound's unique combination of functional groups and structural features makes it a subject of interest for further research and application in various chemical fields.

(3-chloro-5-fluoro-phenyl)-cyclohexyl-methanone

898769-36-3: (3-Chloro-5-fluoro-phenyl)-cyclohexyl-methanone, with the CAS number 898769-36-3, is an organic compound characterized by its unique molecular structure, which includes a cyclohexyl group and a phenyl ring substituted with both chlorine and fluorine atoms. This compound typically exhibits properties associated with halogenated aromatic compounds, such as increased lipophilicity and potential biological activity. The presence of the chloro and fluoro substituents can influence its reactivity, stability, and interaction with biological systems, making it of interest in medicinal chemistry and material science. The cyclohexyl moiety contributes to its steric bulk, which may affect its conformational flexibility and overall molecular interactions. Additionally, the compound may exhibit specific solubility characteristics, depending on the solvent used, and could participate in various chemical reactions, including nucleophilic substitutions or electrophilic aromatic substitutions. Overall, this compound's unique combination of functional groups and structural features makes it a subject of interest for further research and application in various chemical fields.

CAS 898769-36-3

(3-chloro-5-fluoro-phenyl)-cyclohexyl-methanone

3-chloro-5-fluorophenyl cyclohexyl ketone

Ref: 10-F204189