N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide - CAS 1225936-91-3 Catalog number: BADC-00536

N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide is a versatile chemical compound with wide-ranging potential applications across various scientific and industrial fields. Its unique chemical structure, featuring functional groups like a formyl and phenoxy moiety, makes it valuable in areas from drug development to materials science.

Medicinal Chemistry: N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide shows significant potential in medicinal chemistry. The presence of its benzamide and aldehyde functional groups allows it to serve as a pharmacophore in drug design, interacting with diverse biological targets. This compound can be optimized through structural modifications to enhance its pharmacological activity and specificity. It holds promise as a lead compound for developing treatments for diseases such as cancer, inflammation, or neurological disorders, by targeting specific enzymes or receptors.

Synthetic Organic Chemistry: As an intermediate, N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide plays a critical role in synthetic organic chemistry. Its unique molecular structure makes it an ideal building block for constructing more complex molecules with desired functional groups. Its reactivity, particularly from the aldehyde and phenoxy functionalities, enables it to participate in diverse organic reactions. This property supports the synthesis of advanced materials and pharmaceutical compounds, aiding in the optimization of chemical processes across multiple industries.

Biochemical Research: In biochemical studies, N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide serves as a valuable tool for investigating enzyme mechanisms and molecular interactions. By studying its binding affinity with specific proteins or enzymes, researchers can gain deeper insights into biochemical pathways and molecular dynamics. Such studies are essential for understanding disease mechanisms and identifying potential therapeutic targets. Moreover, its functional groups make it suitable for tagging and analyzing target proteins, facilitating advancements in proteomics and molecular biology.

Material Science: N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide also demonstrates significant utility in material science. Incorporating this compound into polymers or coatings can enhance material properties such as thermal stability, mechanical strength, and chemical resistance. These improvements are particularly valuable in industries like electronics, automotive, and aerospace. Additionally, its phenoxy moiety may exhibit excellent performance in surface functionalization, making it a prime candidate for optimizing biomedical devices, biosensors, and medical implants.