3-Chloro-2-(cyclopropylmethoxy)-5-ethylbenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of a chloro substituent and a cyclopropylmethoxy group contributes to its unique reactivity and potential applications in organic synthesis. The ethyl group enhances its hydrophobic character, influencing its solubility and interaction with biological systems. This compound may exhibit interesting properties such as antimicrobial or antifungal activity, making it a candidate for further research in medicinal chemistry. Its molecular structure suggests potential for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the chloro group and the electron-donating properties of the methoxy group. The specific arrangement of substituents on the benzene ring can also affect its physical properties, such as boiling point and melting point, as well as its reactivity in different chemical environments. Overall, 3-chloro-2-(cyclopropylmethoxy)-5-ethylbenzaldehyde represents a versatile compound with potential applications in various fields of chemistry.

3-CHLORO-2-(CYCLOPROPYLMETHOXY)-5-ETHYLBENZALDEHYDE

883519-56-0: 3-Chloro-2-(cyclopropylmethoxy)-5-ethylbenzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group. The presence of a chloro substituent and a cyclopropylmethoxy group contributes to its unique reactivity and potential applications in organic synthesis. The ethyl group enhances its hydrophobic character, influencing its solubility and interaction with biological systems. This compound may exhibit interesting properties such as antimicrobial or antifungal activity, making it a candidate for further research in medicinal chemistry. Its molecular structure suggests potential for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the chloro group and the electron-donating properties of the methoxy group. The specific arrangement of substituents on the benzene ring can also affect its physical properties, such as boiling point and melting point, as well as its reactivity in different chemical environments. Overall, 3-chloro-2-(cyclopropylmethoxy)-5-ethylbenzaldehyde represents a versatile compound with potential applications in various fields of chemistry.

CAS 883519-56-0

3-CHLORO-2-(CYCLOPROPYLMETHOXY)-5-ETHYLBENZALDEHYDE