4-Fluoro-7-methoxy-1-indanone is an organic compound characterized by its indanone structure, which features a fused benzene and cyclopentanone ring system. The presence of a fluorine atom at the 4-position and a methoxy group at the 7-position contributes to its unique chemical properties. This compound typically exhibits moderate polarity due to the electronegative fluorine and the methoxy group, influencing its solubility in various organic solvents. It may participate in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the fluorine atom, while the methoxy group can act as an electron-donating substituent, affecting reactivity. Additionally, 4-fluoro-7-methoxy-1-indanone may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its stability and reactivity can be influenced by the specific conditions under which it is handled, including temperature and the presence of other reactive species. Overall, this compound represents a valuable scaffold for further chemical exploration and potential applications in pharmaceuticals.

4-Fluoro-7-Methoxy-1-indanone

127033-13-0: 4-Fluoro-7-methoxy-1-indanone is an organic compound characterized by its indanone structure, which features a fused benzene and cyclopentanone ring system. The presence of a fluorine atom at the 4-position and a methoxy group at the 7-position contributes to its unique chemical properties. This compound typically exhibits moderate polarity due to the electronegative fluorine and the methoxy group, influencing its solubility in various organic solvents. It may participate in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the fluorine atom, while the methoxy group can act as an electron-donating substituent, affecting reactivity. Additionally, 4-fluoro-7-methoxy-1-indanone may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its stability and reactivity can be influenced by the specific conditions under which it is handled, including temperature and the presence of other reactive species. Overall, this compound represents a valuable scaffold for further chemical exploration and potential applications in pharmaceuticals.

1H-Inden-1-one, 4-fluoro-2,3-dihydro-7-methoxy-

<p>4-Fluoro-7-methoxy-2,3-dihydro-1H-inden-1-one</p>

CAS 127033-13-0

4-Fluoro-7-Methoxy-1-indanone

1H-Inden-1-one, 4-fluoro-2,3-dihydro-7-methoxy-

Ref: IN-DA000WLQ

4-Fluoro-7-methoxy-2,3-dihydro-1H-inden-1-one

Ref: 54-PC1002426

4-Fluoro-7-methoxy-2,3-dihydro-1H-inden-1-one

Ref: 10-F690242