6-Chloro-1-[3-(trifluoromethyl)phenyl]hexan-1-one is an organic compound characterized by its unique structure, which includes a hexanone backbone substituted with a chloro group and a trifluoromethylphenyl moiety. The presence of the chloro substituent introduces a polar functional group, which can influence the compound's reactivity and solubility in various solvents. The trifluoromethyl group is known for its electron-withdrawing properties, enhancing the compound's lipophilicity and potentially affecting its biological activity. This compound is likely to exhibit moderate stability under standard conditions, but its reactivity may increase in the presence of nucleophiles or under acidic or basic conditions. Its molecular structure suggests potential applications in pharmaceuticals or agrochemicals, where such substituents can modulate biological interactions. Additionally, the compound's CAS number, 898783-58-9, allows for easy identification and retrieval of information regarding its properties, safety data, and regulatory status in chemical databases. Overall, this compound exemplifies the complexity and diversity of organic chemistry, particularly in the design of molecules with specific functional characteristics.

6-chloro-1-[3-(trifluoromethyl)phenyl]hexan-1-one

898783-58-9: 6-Chloro-1-[3-(trifluoromethyl)phenyl]hexan-1-one is an organic compound characterized by its unique structure, which includes a hexanone backbone substituted with a chloro group and a trifluoromethylphenyl moiety. The presence of the chloro substituent introduces a polar functional group, which can influence the compound's reactivity and solubility in various solvents. The trifluoromethyl group is known for its electron-withdrawing properties, enhancing the compound's lipophilicity and potentially affecting its biological activity. This compound is likely to exhibit moderate stability under standard conditions, but its reactivity may increase in the presence of nucleophiles or under acidic or basic conditions. Its molecular structure suggests potential applications in pharmaceuticals or agrochemicals, where such substituents can modulate biological interactions. Additionally, the compound's CAS number, 898783-58-9, allows for easy identification and retrieval of information regarding its properties, safety data, and regulatory status in chemical databases. Overall, this compound exemplifies the complexity and diversity of organic chemistry, particularly in the design of molecules with specific functional characteristics.

CAS 898783-58-9

6-chloro-1-[3-(trifluoromethyl)phenyl]hexan-1-one

6-chloro-1-oxo-1-(3-trifluoromethylphenyl)hexane

Ref: 10-F203721