3-Chloro-5-ethoxy-4-(prop-2-en-1-yloxy)benzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of a chloro substituent at the 3-position and an ethoxy group at the 5-position on the benzene ring contributes to its reactivity and solubility properties. The compound also features a prop-2-en-1-yloxy group, which introduces an allylic ether functionality, enhancing its potential for further chemical transformations. This compound is likely to exhibit moderate polarity due to the combination of hydrophobic aromatic and hydrophilic ether and aldehyde groups. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it of interest in synthetic organic chemistry. Additionally, its unique structure may confer specific biological activities, warranting investigation in medicinal chemistry. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks or environmental hazards.

3-chloro-5-ethoxy-4-(prop-2-en-1-yloxy)benzaldehyde

443291-94-9: 3-Chloro-5-ethoxy-4-(prop-2-en-1-yloxy)benzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of a chloro substituent at the 3-position and an ethoxy group at the 5-position on the benzene ring contributes to its reactivity and solubility properties. The compound also features a prop-2-en-1-yloxy group, which introduces an allylic ether functionality, enhancing its potential for further chemical transformations. This compound is likely to exhibit moderate polarity due to the combination of hydrophobic aromatic and hydrophilic ether and aldehyde groups. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it of interest in synthetic organic chemistry. Additionally, its unique structure may confer specific biological activities, warranting investigation in medicinal chemistry. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks or environmental hazards.

CAS 443291-94-9

3-chloro-5-ethoxy-4-(prop-2-en-1-yloxy)benzaldehyde

4-(allyloxy)-3-chloro-5-ethoxybenzaldehyde

Ref: 10-F314958

4-(Allyloxy)-3-chloro-5-ethoxybenzaldehyde

Ref: 3D-TSA29194