1-(4-Fluorophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one, also known by its CAS number 2965-64-2, is an organic compound characterized by its conjugated system, which includes a prop-2-en-1-one backbone. This compound features two aromatic rings: one with a fluorine substituent and the other with a methoxy group, contributing to its unique electronic properties. The presence of the fluorine atom enhances the compound's lipophilicity and can influence its reactivity and interaction with biological targets. The methoxy group, being an electron-donating substituent, can stabilize the molecule and affect its spectral properties. This compound may exhibit interesting photophysical properties, making it a candidate for applications in organic electronics, dyes, or as a potential pharmaceutical intermediate. Its structural features suggest potential reactivity in various chemical reactions, including electrophilic substitutions and Michael additions. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

1-(4-fluorophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

2965-64-2: 1-(4-Fluorophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one, also known by its CAS number 2965-64-2, is an organic compound characterized by its conjugated system, which includes a prop-2-en-1-one backbone. This compound features two aromatic rings: one with a fluorine substituent and the other with a methoxy group, contributing to its unique electronic properties. The presence of the fluorine atom enhances the compound's lipophilicity and can influence its reactivity and interaction with biological targets. The methoxy group, being an electron-donating substituent, can stabilize the molecule and affect its spectral properties. This compound may exhibit interesting photophysical properties, making it a candidate for applications in organic electronics, dyes, or as a potential pharmaceutical intermediate. Its structural features suggest potential reactivity in various chemical reactions, including electrophilic substitutions and Michael additions. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

CAS 2965-64-2

1-(4-fluorophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

2-PROPEN-1-ONE, 1-(4-FLUOROPHENYL)-3-(4-METHOXYPHENYL)-

Ref: IN-DA002Z08

4-Methoxy-4'-fluorochalcone

Ref: 54-PC3944

4-Methoxy-4′-fluorochalcone

Ref: 10-F005223