N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide is a fluorophenoxy-containing aldehyde ADC linker optimized for selective bioorthogonal antibody conjugation, enhancing payload attachment and therapeutic efficacy in ADCs.
Structure of 1225705-45-2
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N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide, a compound of notable interest, has been increasingly explored for its potential applications in the pharmaceutical industry. This chemical entity is often examined in the context of drug development due to its structural features, which may facilitate interactions with specific biological targets. The presence of the formyl group alongside the fluoro-substituted phenoxy moiety suggests potential utility in the synthesis of bioactive molecules, where modifications in such structures can lead to variations in activity or selectivity against certain biological pathways. Through these studies, researchers aim to uncover new therapeutic avenues, especially in challenging diseases that require more effective intervention strategies.
Furthermore, the compound's ability to influence interactions at the molecular level makes it an attractive candidate in medicinal chemistry research. Scientists focus on the compound’s role as a building block in constructing novel pharmacophores, which are parts of molecules responsible for their biological activity. By tweaking its structure, researchers can systematically evaluate changes in biological activity, offering insights into the relationships between chemical structure and biological function. This is particularly valuable in designing selective agents that can modulate specific proteins or enzymes implicated in disease processes, thereby advancing the development of more precise and targeted therapies.
In the realm of chemical biology, N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide might also serve as a probe or a scaffold for designing analytical tools. Its structural attributes allow it to be incorporated into larger molecular frameworks that can be used to explore complex biological environments. Such tools are essential for visualizing cellular processes or for identifying and validating new biological targets. Consequently, this enhances our understanding of cellular pathways and mechanisms at a molecular level, enabling researchers to devise better strategies for diagnostic or therapeutic purposes.
Lastly, the compound's versatile chemistry allows it to be utilized in a variety of synthetic methodologies, expanding its applicability beyond pharmaceuticals into fields such as materials science. Incorporating this compound into polymers or advanced materials could impart novel properties, potentially leading to innovative applications in electronics, coatings, or biocompatible materials. The ability to blend function with form is a driving force in material innovation, and N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide presents exciting possibilities in this aspect, inviting multidisciplinary research efforts aimed at harnessing its full potential.
Catalog | Product Name | CAS | Inquiry |
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BADC-00523 | N-(2-(2-Chloroethoxy)ethyl)-4-Formylbenzamide | 1137575-49-5 | |
BADC-00531 | N-(2-(4-Fluorophenoxy)ethyl)-4-Formylbenzamide | 1225588-22-6 | |
BADC-00532 | N-(2-(3-Fluorophenoxy)ethyl)-4-Formylbenzamide | 1225588-29-3 | |
BADC-00534 | N-(2-(3-Ethylphenoxy)ethyl)-4-Formylbenzamide | 1225790-49-7 | |
BADC-00535 | N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide | 1225790-59-9 | |
BADC-00536 | N-(2-(2,6-Dimethylphenoxy)ethyl)-4-Formylbenzamide | 1225936-91-3 | |
BADC-00539 | N-(2-(2-Chlorophenoxy)ethyl)-4-Formylbenzamide | 1225972-65-5 | |
BADC-00540 | N-(2-((2,3-Dihydro-1H-Inden-5-yl)oxy)ethyl)-4-Formylbenzamide | 1225979-81-6 | |
BADC-00541 | N-(2-(Benzo[d][1,3]dioxol-5-yloxy)ethyl)-4-Formylbenzamide | 1226006-03-6 | |
BADC-00543 | N-(2-(3-Ethoxyphenoxy)ethyl)-4-Formylbenzamide | 1226006-55-8 |
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