3-(2-Chloro-6-fluorophenyl)-1-(4-fluorophenyl)-2-propen-1-one is an organic compound characterized by its unique structure, which includes a propenone moiety with two aromatic rings substituted with halogen atoms. The presence of a 2-chloro and a 4-fluoro group on the phenyl rings contributes to its chemical reactivity and potential biological activity. This compound is likely to exhibit properties typical of α,β-unsaturated carbonyl compounds, such as the ability to undergo Michael addition reactions and other nucleophilic attacks due to the electrophilic nature of the carbonyl group. Its halogen substituents can influence its lipophilicity, stability, and interaction with biological targets, making it of interest in medicinal chemistry. Additionally, the compound may exhibit specific spectral characteristics in techniques such as NMR and IR spectroscopy, which can be used for its identification and characterization. Overall, the unique combination of substituents and functional groups in this compound suggests potential applications in pharmaceuticals or agrochemicals, although specific biological activities would require further investigation.

3-(2-CHLORO-6-FLUOROPHENYL)-1-(4-FLUOROPHENYL)-2-PROPEN-1-ONE

1164538-77-5: 3-(2-Chloro-6-fluorophenyl)-1-(4-fluorophenyl)-2-propen-1-one is an organic compound characterized by its unique structure, which includes a propenone moiety with two aromatic rings substituted with halogen atoms. The presence of a 2-chloro and a 4-fluoro group on the phenyl rings contributes to its chemical reactivity and potential biological activity. This compound is likely to exhibit properties typical of α,β-unsaturated carbonyl compounds, such as the ability to undergo Michael addition reactions and other nucleophilic attacks due to the electrophilic nature of the carbonyl group. Its halogen substituents can influence its lipophilicity, stability, and interaction with biological targets, making it of interest in medicinal chemistry. Additionally, the compound may exhibit specific spectral characteristics in techniques such as NMR and IR spectroscopy, which can be used for its identification and characterization. Overall, the unique combination of substituents and functional groups in this compound suggests potential applications in pharmaceuticals or agrochemicals, although specific biological activities would require further investigation.

CAS 1164538-77-5

3-(2-CHLORO-6-FLUOROPHENYL)-1-(4-FLUOROPHENYL)-2-PROPEN-1-ONE

(2E)-3-(2-chloro-6-fluorophenyl)-1-(4-fluorophenyl)prop-2-en-1-one

Ref: 10-F523863