3-Chloro-5-methoxy-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 a methoxy group at the 5-position on the benzene ring contributes to its reactivity and solubility properties. The prop-2-en-1-yloxy group, attached at the 4-position, introduces an allylic ether functionality, which can participate in various chemical reactions, such as nucleophilic substitutions or polymerization processes. This compound is likely to exhibit moderate polarity due to the combination of hydrophobic aromatic and hydrophilic functional groups. Its molecular structure suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the compound's unique substituents may influence its biological activity, making it a candidate for further research in medicinal chemistry. As with many organic compounds, safety precautions should be taken when handling it, considering potential toxicity or reactivity.

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

428479-97-4: 3-Chloro-5-methoxy-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 a methoxy group at the 5-position on the benzene ring contributes to its reactivity and solubility properties. The prop-2-en-1-yloxy group, attached at the 4-position, introduces an allylic ether functionality, which can participate in various chemical reactions, such as nucleophilic substitutions or polymerization processes. This compound is likely to exhibit moderate polarity due to the combination of hydrophobic aromatic and hydrophilic functional groups. Its molecular structure suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the compound's unique substituents may influence its biological activity, making it a candidate for further research in medicinal chemistry. As with many organic compounds, safety precautions should be taken when handling it, considering potential toxicity or reactivity.

CAS 428479-97-4

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

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

Ref: IN-DA00BZ9M

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

Ref: 3D-DSA47997