2-Phenyl-1-[4-(trifluoromethyl)phenyl]ethanone, with the CAS number 61062-55-3, is an organic compound characterized by its ketone functional group and the presence of both phenyl and trifluoromethyl substituents. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the phenyl groups, which contribute to its stability and reactivity. The trifluoromethyl group is notable for enhancing the lipophilicity and biological activity of the molecule, making it of interest in various fields, including pharmaceuticals and agrochemicals. The presence of the ketone functional group suggests potential reactivity in nucleophilic addition reactions. Additionally, the compound may exhibit interesting optical and electronic properties due to its structural features. Its synthesis often involves methods typical for constructing ketones, such as Friedel-Crafts acylation. Safety data should be consulted for handling, as the trifluoromethyl group can impart unique toxicological properties.

2-phenyl-1-[4-(trifluoromethyl)phenyl]ethanone

61062-55-3: 2-Phenyl-1-[4-(trifluoromethyl)phenyl]ethanone, with the CAS number 61062-55-3, is an organic compound characterized by its ketone functional group and the presence of both phenyl and trifluoromethyl substituents. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the phenyl groups, which contribute to its stability and reactivity. The trifluoromethyl group is notable for enhancing the lipophilicity and biological activity of the molecule, making it of interest in various fields, including pharmaceuticals and agrochemicals. The presence of the ketone functional group suggests potential reactivity in nucleophilic addition reactions. Additionally, the compound may exhibit interesting optical and electronic properties due to its structural features. Its synthesis often involves methods typical for constructing ketones, such as Friedel-Crafts acylation. Safety data should be consulted for handling, as the trifluoromethyl group can impart unique toxicological properties.

<p>Applications 2-Phenyl-4’-trifluoromethylacetophenone, is used in the preparation of arylketones via palladium-tedicyp-catalyzed Heck reaction.<br>References Battace, A., et al.: Eur. J. Org. Chem., 19, 3122 (2007)<br></p>

CAS 61062-55-3

2-phenyl-1-[4-(trifluoromethyl)phenyl]ethanone

2-Phenyl-4’-trifluoromethylacetophenone

Ref: TR-P337440