3-(4-Methoxyphenyl)-1-(4-nitrophenyl)prop-2-en-1-one, also known by its CAS number 6552-62-1, is an organic compound characterized by its conjugated system, which includes a prop-2-en-1-one backbone. This compound features two aromatic substituents: a methoxy group on one phenyl ring and a nitro group on the other, contributing to its unique electronic properties. The presence of the methoxy group enhances the electron density on the aromatic ring, while the nitro group, being electron-withdrawing, can influence the compound's reactivity and stability. This compound is typically yellow in color and may exhibit fluorescence, making it of interest in various applications, including organic synthesis and materials science. Its structural features suggest potential uses in dye chemistry and as a precursor for further chemical modifications. Additionally, the compound's reactivity can be attributed to the α,β-unsaturated carbonyl system, which is susceptible to nucleophilic attack, making it a valuable intermediate in organic synthesis.

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

6552-62-1: 3-(4-Methoxyphenyl)-1-(4-nitrophenyl)prop-2-en-1-one, also known by its CAS number 6552-62-1, is an organic compound characterized by its conjugated system, which includes a prop-2-en-1-one backbone. This compound features two aromatic substituents: a methoxy group on one phenyl ring and a nitro group on the other, contributing to its unique electronic properties. The presence of the methoxy group enhances the electron density on the aromatic ring, while the nitro group, being electron-withdrawing, can influence the compound's reactivity and stability. This compound is typically yellow in color and may exhibit fluorescence, making it of interest in various applications, including organic synthesis and materials science. Its structural features suggest potential uses in dye chemistry and as a precursor for further chemical modifications. Additionally, the compound's reactivity can be attributed to the α,β-unsaturated carbonyl system, which is susceptible to nucleophilic attack, making it a valuable intermediate in organic synthesis.

CAS 6552-62-1

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

(2E)-3-(4-methoxyphenyl)-1-(4-nitrophenyl)prop-2-en-1-one

Ref: 10-F523628