2-[(2-Fluorobenzyl)oxy]naphthalene-1-carbaldehyde is an organic compound characterized by its complex structure, which includes a naphthalene ring system substituted with a fluorobenzyl ether and an aldehyde functional group. This compound typically exhibits properties associated with aromatic compounds, such as stability and potential for electrophilic substitution reactions. The presence of the fluorine atom can influence its reactivity and polarity, potentially enhancing its lipophilicity and affecting its biological activity. The aldehyde group contributes to its reactivity, allowing for further functionalization or participation in condensation reactions. In terms of physical properties, compounds of this nature may be expected to be solid at room temperature, with moderate solubility in organic solvents. Its applications could span various fields, including medicinal chemistry, where such derivatives may serve as intermediates in the synthesis of pharmaceuticals or as probes in biological studies. Overall, the unique combination of functional groups in 2-[(2-fluorobenzyl)oxy]naphthalene-1-carbaldehyde makes it a compound of interest for further research and application.

2-[(2-fluorobenzyl)oxy]naphthalene-1-carbaldehyde

725276-88-0: 2-[(2-Fluorobenzyl)oxy]naphthalene-1-carbaldehyde is an organic compound characterized by its complex structure, which includes a naphthalene ring system substituted with a fluorobenzyl ether and an aldehyde functional group. This compound typically exhibits properties associated with aromatic compounds, such as stability and potential for electrophilic substitution reactions. The presence of the fluorine atom can influence its reactivity and polarity, potentially enhancing its lipophilicity and affecting its biological activity. The aldehyde group contributes to its reactivity, allowing for further functionalization or participation in condensation reactions. In terms of physical properties, compounds of this nature may be expected to be solid at room temperature, with moderate solubility in organic solvents. Its applications could span various fields, including medicinal chemistry, where such derivatives may serve as intermediates in the synthesis of pharmaceuticals or as probes in biological studies. Overall, the unique combination of functional groups in 2-[(2-fluorobenzyl)oxy]naphthalene-1-carbaldehyde makes it a compound of interest for further research and application.

CAS 725276-88-0

2-[(2-fluorobenzyl)oxy]naphthalene-1-carbaldehyde

2-[(2-fluorobenzyl)oxy]-1-naphthaldehyde

Ref: 10-F315438