2-(Methylsulfonyl)-1-[4-(trifluoromethyl)phenyl]ethanone, with the CAS number 386715-52-2, is an organic compound characterized by its unique functional groups and structural features. It contains a methylsulfonyl group, which contributes to its polar nature and potential solubility in polar solvents. The presence of a trifluoromethyl group on the phenyl ring enhances its lipophilicity and can influence its reactivity and biological activity. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals or agrochemicals, particularly due to the presence of the sulfonyl and trifluoromethyl groups, which are known to impart specific biological properties. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it of interest in synthetic organic chemistry. Safety data should be consulted for handling and usage, as compounds with trifluoromethyl groups can exhibit unique toxicological profiles.

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

386715-52-2: 2-(Methylsulfonyl)-1-[4-(trifluoromethyl)phenyl]ethanone, with the CAS number 386715-52-2, is an organic compound characterized by its unique functional groups and structural features. It contains a methylsulfonyl group, which contributes to its polar nature and potential solubility in polar solvents. The presence of a trifluoromethyl group on the phenyl ring enhances its lipophilicity and can influence its reactivity and biological activity. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals or agrochemicals, particularly due to the presence of the sulfonyl and trifluoromethyl groups, which are known to impart specific biological properties. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it of interest in synthetic organic chemistry. Safety data should be consulted for handling and usage, as compounds with trifluoromethyl groups can exhibit unique toxicological profiles.

CAS 386715-52-2

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

2-(Methylsulfonyl)-1-(4-(trifluoromethyl)phenyl)ethanone

Ref: IN-DA00BYQ4

2-Methylsulfonyl-1-(4-trifluoromethylphenyl)ethanone

Ref: 10-F009291

4-(Methylsulphonylacetyl)benzotrifluoride

Ref: 54-PC5551