2-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 2-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 polymerizations. 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 presence of both electron-withdrawing (chloro) and electron-donating (methoxy) groups can influence its electronic properties, making it a candidate for studies in reactivity and mechanism exploration in organic chemistry.

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

692279-00-8: 2-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 2-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 polymerizations. 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 presence of both electron-withdrawing (chloro) and electron-donating (methoxy) groups can influence its electronic properties, making it a candidate for studies in reactivity and mechanism exploration in organic chemistry.

CAS 692279-00-8

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

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

Ref: 3D-SCB27900