3-(4-Chlorophenoxy)benzaldehyde is an organic compound characterized by its aromatic structure, which includes a benzaldehyde group and a chlorophenoxy substituent. The presence of the aldehyde functional group (-CHO) indicates that it can participate in various chemical reactions, such as oxidation and condensation. The chlorophenoxy moiety contributes to the compound's overall polarity and can influence its reactivity and solubility in different solvents. This compound typically appears as a pale yellow to light brown liquid or solid, depending on its purity and form. It is often used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to act as an intermediate in various chemical reactions. Additionally, the chlorine atom in the para position can enhance the compound's biological activity and modulate its electronic properties. Safety precautions should be taken when handling this substance, as it may pose health risks if inhaled or ingested, and proper storage conditions should be maintained to ensure stability.

3-(4-Chlorophenoxy)benzaldehyde

69770-20-3: Benzaldehyde, 3-(4-chlorophenoxy)-, m-(p-Chlorophenoxy)benzaldehyde, 3-(4-Chlorophenoxy)benzaldehyde

3-(4-chlorophenoxy)benzaldehyde is a fatty acid that has been shown to be useful in treating neuropathic pain and tuberculosis. It is synthesized by the hydrolase activity of an enzyme called fatty acid amide hydrolase (FAAH), which degrades endocannabinoids such as anandamide, resulting in anti-neuropathic effects. The spirocyclic ring system of 3-(4-chlorophenoxy)benzaldehyde has also been shown to have antitubercular activity against Mycobacterium tuberculosis. This compound can be activated by ethanolamide, leading to its use as a cellular amide.

CAS 69770-20-3: 3-(4-Chlorophenoxy)benzaldehyde

3-(4-Chlorophenoxy)benzaldehyde

Ref: IN-DA003I3V

3-(4-chlorophenoxy)benzaldehyde

Ref: 3D-UCA77020

3-(4-Chlorophenoxy)benzaldehyde

Ref: 10-F678965