3-Bromo-5-ethoxy-4-hydroxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a bromine atom, an ethoxy group, and a hydroxy group attached to a benzaldehyde moiety. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and polarity. The ethoxy group contributes to the compound's hydrophobic characteristics, while the hydroxy group enhances its solubility in polar solvents and can participate in hydrogen bonding. This compound typically exhibits properties such as moderate to high melting and boiling points due to its molecular interactions. It may also display UV-Vis absorbance characteristics due to the conjugated system of the aromatic ring. Additionally, 3-bromo-5-ethoxy-4-hydroxybenzaldehyde can serve as a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, owing to its functional groups that allow for further chemical modifications. Its reactivity can be influenced by the electron-withdrawing effects of the bromine and the electron-donating effects of the ethoxy and hydroxy groups.

3-bromo-5-ethoxy-4-hydroxybenzaldehyde

3111-37-3: 3-Bromo-5-ethoxy-4-hydroxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a bromine atom, an ethoxy group, and a hydroxy group attached to a benzaldehyde moiety. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and polarity. The ethoxy group contributes to the compound's hydrophobic characteristics, while the hydroxy group enhances its solubility in polar solvents and can participate in hydrogen bonding. This compound typically exhibits properties such as moderate to high melting and boiling points due to its molecular interactions. It may also display UV-Vis absorbance characteristics due to the conjugated system of the aromatic ring. Additionally, 3-bromo-5-ethoxy-4-hydroxybenzaldehyde can serve as a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, owing to its functional groups that allow for further chemical modifications. Its reactivity can be influenced by the electron-withdrawing effects of the bromine and the electron-donating effects of the ethoxy and hydroxy groups.

CAS 3111-37-3

3-bromo-5-ethoxy-4-hydroxybenzaldehyde

3-BROMO-5-ETHOXY-4-HYDROXYBENZALDEHYDE

Ref: IN-DA003J2P

3-Bromo-5-ethoxy-4-hydroxybenzaldehyde

Ref: 54-OR22077

3-Bromo-5-ethoxy-4-hydroxy-benzaldehyde

Ref: 10-F031718