3-Fluoro-5-hydroxybenzaldehyde is an organic compound characterized by the presence of a fluorine atom, a hydroxyl group, and an aldehyde functional group attached to a benzene ring. The fluorine atom is located at the meta position relative to the hydroxyl group, which influences the compound's reactivity and polarity. The hydroxyl group contributes to its potential as a hydrogen bond donor, enhancing its solubility in polar solvents. As an aldehyde, it exhibits typical reactivity associated with carbonyl compounds, including nucleophilic addition reactions. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in synthesizing more complex molecules or as a building block in organic synthesis. Its unique combination of functional groups can also impart specific biological activities, making it a candidate for further research in drug development. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with its use.

3-fluoro-5-hydroxybenzaldehyde

1023290-12-1: 3-Fluoro-5-hydroxybenzaldehyde is an organic compound characterized by the presence of a fluorine atom, a hydroxyl group, and an aldehyde functional group attached to a benzene ring. The fluorine atom is located at the meta position relative to the hydroxyl group, which influences the compound's reactivity and polarity. The hydroxyl group contributes to its potential as a hydrogen bond donor, enhancing its solubility in polar solvents. As an aldehyde, it exhibits typical reactivity associated with carbonyl compounds, including nucleophilic addition reactions. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in synthesizing more complex molecules or as a building block in organic synthesis. Its unique combination of functional groups can also impart specific biological activities, making it a candidate for further research in drug development. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with its use.

CAS 1023290-12-1

3-fluoro-5-hydroxybenzaldehyde

Benzaldehyde, 3-fluoro-5-hydroxy-

Ref: IN-DA00076Q

3-Fluoro-5-hydroxybenzaldehyde

Ref: 54-PC52056

3-Fluoro-5-hydroxybenzaldehyde

Ref: 10-F076022