4-[(2,6-Dichlorobenzyl)oxy]benzaldehyde, with the CAS number 166049-76-9, is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and a dichlorobenzyl ether moiety. This compound features a benzene ring substituted with an aldehyde group (-CHO) and an ether linkage to a 2,6-dichlorobenzyl group, contributing to its unique chemical properties. The presence of chlorine atoms enhances its reactivity and may influence its biological activity, making it of interest in various fields, including medicinal chemistry and materials science. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its synthesis often involves electrophilic aromatic substitution reactions or etherification processes. Due to its structural characteristics, it may also exhibit specific optical properties and potential applications in organic synthesis or as an intermediate in the production of more complex molecules. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

4-[(2,6-dichlorobenzyl)oxy]benzaldehyde

166049-76-9: 4-[(2,6-Dichlorobenzyl)oxy]benzaldehyde, with the CAS number 166049-76-9, is an organic compound characterized by its aromatic structure, which includes a benzaldehyde functional group and a dichlorobenzyl ether moiety. This compound features a benzene ring substituted with an aldehyde group (-CHO) and an ether linkage to a 2,6-dichlorobenzyl group, contributing to its unique chemical properties. The presence of chlorine atoms enhances its reactivity and may influence its biological activity, making it of interest in various fields, including medicinal chemistry and materials science. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its synthesis often involves electrophilic aromatic substitution reactions or etherification processes. Due to its structural characteristics, it may also exhibit specific optical properties and potential applications in organic synthesis or as an intermediate in the production of more complex molecules. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

CAS 166049-76-9

4-[(2,6-dichlorobenzyl)oxy]benzaldehyde

4-[(2,6-Dichlorobenzyl)oxy]benzaldehyde

Ref: IN-DA001WGD

4-[(2,6-dichlorobenzyl)oxy]benzaldehyde

Ref: 10-F307606