3-[(4-Fluorobenzyl)oxy]-4-methoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a methoxy group and a fluorobenzyl ether moiety. The presence of the aldehyde functional group contributes to its reactivity, making it a potential candidate for various chemical reactions, such as condensation and nucleophilic addition. The fluorine atom in the para position of the benzyl group can influence the compound's electronic properties, potentially enhancing its reactivity and solubility in organic solvents. This compound may exhibit interesting biological activities due to its structural features, making it of interest in medicinal chemistry and drug development. Additionally, its unique combination of functional groups allows for potential applications in materials science and organic synthesis. The compound's stability, solubility, and reactivity can vary based on environmental conditions, such as pH and temperature, which are important considerations in practical applications. Overall, 3-[(4-fluorobenzyl)oxy]-4-methoxybenzaldehyde is a versatile compound with significant potential in various fields of chemistry.

3-[(4-fluorobenzyl)oxy]-4-methoxybenzaldehyde

351066-28-9: 3-[(4-Fluorobenzyl)oxy]-4-methoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a methoxy group and a fluorobenzyl ether moiety. The presence of the aldehyde functional group contributes to its reactivity, making it a potential candidate for various chemical reactions, such as condensation and nucleophilic addition. The fluorine atom in the para position of the benzyl group can influence the compound's electronic properties, potentially enhancing its reactivity and solubility in organic solvents. This compound may exhibit interesting biological activities due to its structural features, making it of interest in medicinal chemistry and drug development. Additionally, its unique combination of functional groups allows for potential applications in materials science and organic synthesis. The compound's stability, solubility, and reactivity can vary based on environmental conditions, such as pH and temperature, which are important considerations in practical applications. Overall, 3-[(4-fluorobenzyl)oxy]-4-methoxybenzaldehyde is a versatile compound with significant potential in various fields of chemistry.

CAS 351066-28-9

3-[(4-fluorobenzyl)oxy]-4-methoxybenzaldehyde

3-[(4-Fluorophenyl)methoxy]-4-methoxybenzaldehyde

Ref: IN-DA007FS0

3-(4-Fluoro-benzyloxy)-4-methoxy-benzaldehyde

Ref: 10-F059908