3,5-Dichloro-4-(prop-2-en-1-yloxy)benzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and a prop-2-en-1-yloxy substituent. The presence of two chlorine atoms at the 3 and 5 positions of the benzene ring contributes to its reactivity and potential applications in various chemical reactions, including electrophilic aromatic substitution. The aldehyde group (-CHO) is known for its reactivity, particularly in condensation reactions and as a precursor in the synthesis of other organic compounds. The prop-2-en-1-yloxy group introduces a vinyl ether functionality, which can participate in further chemical transformations, such as polymerization or cross-coupling reactions. This compound may exhibit biological activity, making it of interest in medicinal chemistry and agrochemicals. Its physical properties, such as solubility and boiling point, would depend on the specific molecular interactions and the presence of functional groups. Overall, 3,5-dichloro-4-(prop-2-en-1-yloxy)benzaldehyde is a versatile compound with potential applications in synthetic organic chemistry.

3,5-dichloro-4-(prop-2-en-1-yloxy)benzaldehyde

27164-07-4: 3,5-Dichloro-4-(prop-2-en-1-yloxy)benzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and a prop-2-en-1-yloxy substituent. The presence of two chlorine atoms at the 3 and 5 positions of the benzene ring contributes to its reactivity and potential applications in various chemical reactions, including electrophilic aromatic substitution. The aldehyde group (-CHO) is known for its reactivity, particularly in condensation reactions and as a precursor in the synthesis of other organic compounds. The prop-2-en-1-yloxy group introduces a vinyl ether functionality, which can participate in further chemical transformations, such as polymerization or cross-coupling reactions. This compound may exhibit biological activity, making it of interest in medicinal chemistry and agrochemicals. Its physical properties, such as solubility and boiling point, would depend on the specific molecular interactions and the presence of functional groups. Overall, 3,5-dichloro-4-(prop-2-en-1-yloxy)benzaldehyde is a versatile compound with potential applications in synthetic organic chemistry.

CAS 27164-07-4

3,5-dichloro-4-(prop-2-en-1-yloxy)benzaldehyde

4-(allyloxy)-3,5-dichlorobenzaldehyde

Ref: 10-F314962