2-Chloro-5-ethoxy-4-propoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of chlorine, ethoxy, and propoxy substituents on the benzene ring significantly influences its chemical properties and reactivity. The chlorine atom introduces electronegativity, which can affect the compound's polarity and potential for hydrogen bonding. The ethoxy and propoxy groups contribute to the compound's hydrophobic characteristics, potentially impacting its solubility in various solvents. This compound may exhibit moderate to high reactivity due to the aldehyde functional group, which is susceptible to nucleophilic attack. Additionally, the presence of multiple substituents can lead to interesting electronic effects, influencing the compound's behavior in chemical reactions, such as electrophilic aromatic substitution. Overall, 2-chloro-5-ethoxy-4-propoxybenzaldehyde is a versatile compound that may find applications in organic synthesis, pharmaceuticals, or as an intermediate in the production of more complex molecules.

2-chloro-5-ethoxy-4-propoxybenzaldehyde

692275-23-3: 2-Chloro-5-ethoxy-4-propoxybenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of chlorine, ethoxy, and propoxy substituents on the benzene ring significantly influences its chemical properties and reactivity. The chlorine atom introduces electronegativity, which can affect the compound's polarity and potential for hydrogen bonding. The ethoxy and propoxy groups contribute to the compound's hydrophobic characteristics, potentially impacting its solubility in various solvents. This compound may exhibit moderate to high reactivity due to the aldehyde functional group, which is susceptible to nucleophilic attack. Additionally, the presence of multiple substituents can lead to interesting electronic effects, influencing the compound's behavior in chemical reactions, such as electrophilic aromatic substitution. Overall, 2-chloro-5-ethoxy-4-propoxybenzaldehyde is a versatile compound that may find applications in organic synthesis, pharmaceuticals, or as an intermediate in the production of more complex molecules.

CAS 692275-23-3

2-chloro-5-ethoxy-4-propoxybenzaldehyde

2-chloro-5-ethoxy-4-propoxybenzaldehyde

Ref: 10-F315468

2-Chloro-5-ethoxy-4-propoxybenzaldehyde

Ref: 3D-SCB27523