2-(3-Fluorophenyl)-1-(3-iodophenyl)ethanone is an organic compound characterized by its ketone functional group, which is indicated by the presence of the ethanone moiety. This compound features two aromatic rings: one containing a fluorine substituent and the other containing an iodine substituent, both attached to the ethyl carbon of the ketone. The presence of these halogen atoms can influence the compound's reactivity, polarity, and overall stability. Generally, compounds with halogen substituents exhibit unique electronic properties, which can affect their behavior in chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, the presence of the fluorine atom may enhance the compound's lipophilicity, while the iodine atom can introduce steric effects. This compound may be of interest in medicinal chemistry and materials science due to its potential biological activity and utility in synthesizing more complex molecules. As with many organic compounds, safety precautions should be observed when handling it, considering the potential hazards associated with halogenated compounds.

2-(3-fluorophenyl)-1-(3-iodophenyl)ethanone

898784-79-7: 2-(3-Fluorophenyl)-1-(3-iodophenyl)ethanone is an organic compound characterized by its ketone functional group, which is indicated by the presence of the ethanone moiety. This compound features two aromatic rings: one containing a fluorine substituent and the other containing an iodine substituent, both attached to the ethyl carbon of the ketone. The presence of these halogen atoms can influence the compound's reactivity, polarity, and overall stability. Generally, compounds with halogen substituents exhibit unique electronic properties, which can affect their behavior in chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, the presence of the fluorine atom may enhance the compound's lipophilicity, while the iodine atom can introduce steric effects. This compound may be of interest in medicinal chemistry and materials science due to its potential biological activity and utility in synthesizing more complex molecules. As with many organic compounds, safety precautions should be observed when handling it, considering the potential hazards associated with halogenated compounds.

CAS 898784-79-7

2-(3-fluorophenyl)-1-(3-iodophenyl)ethanone

2-(3-fluorophenyl)-3′-iodoacetophenone

Ref: 10-F203829