5-Chloro-1-[3-(trifluoromethoxy)phenyl]pentan-1-one is an organic compound characterized by its complex structure, which includes a pentanone backbone substituted with a chloro group and a trifluoromethoxy phenyl group. The presence of the chloro substituent introduces a halogen, which can influence the compound's reactivity and polarity. The trifluoromethoxy group, consisting of a phenyl ring attached to a -O-CF3 moiety, imparts significant electron-withdrawing properties, enhancing the compound's lipophilicity and potentially affecting its biological activity. This compound may exhibit interesting pharmacological properties due to its unique functional groups, making it a candidate for research in medicinal chemistry. Additionally, its molecular structure suggests potential applications in agrochemicals or as a synthetic intermediate in organic synthesis. The presence of fluorine atoms typically enhances stability and alters the compound's interaction with biological systems, which is a key consideration in drug design and development. Overall, 5-chloro-1-[3-(trifluoromethoxy)phenyl]pentan-1-one represents a versatile compound with potential utility in various chemical applications.

5-chloro-1-[3-(trifluoromethoxy)phenyl]pentan-1-one

898786-25-9: 5-Chloro-1-[3-(trifluoromethoxy)phenyl]pentan-1-one is an organic compound characterized by its complex structure, which includes a pentanone backbone substituted with a chloro group and a trifluoromethoxy phenyl group. The presence of the chloro substituent introduces a halogen, which can influence the compound's reactivity and polarity. The trifluoromethoxy group, consisting of a phenyl ring attached to a -O-CF3 moiety, imparts significant electron-withdrawing properties, enhancing the compound's lipophilicity and potentially affecting its biological activity. This compound may exhibit interesting pharmacological properties due to its unique functional groups, making it a candidate for research in medicinal chemistry. Additionally, its molecular structure suggests potential applications in agrochemicals or as a synthetic intermediate in organic synthesis. The presence of fluorine atoms typically enhances stability and alters the compound's interaction with biological systems, which is a key consideration in drug design and development. Overall, 5-chloro-1-[3-(trifluoromethoxy)phenyl]pentan-1-one represents a versatile compound with potential utility in various chemical applications.

CAS 898786-25-9

5-chloro-1-[3-(trifluoromethoxy)phenyl]pentan-1-one