4-Formyl-N-(2-(2-Methoxy-4-Methylphenoxy)ethyl)benzamide is an aldehyde-bearing ADC linker designed for site-specific conjugation, improving payload attachment and antibody-drug conjugate targeting in cancer therapy.
Structure of 1226006-54-7
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One key application of 4-Formyl-N-(2-(2-Methoxy-4-Methylphenoxy)ethyl)benzamide is in medicinal chemistry, where it serves as an intermediate for the synthesis of pharmaceutical compounds. This compound’s unique structural components, such as the formyl group and the benzamide backbone, allow for the development of a range of biologically active molecules. As an intermediate, it facilitates the creation of drugs aimed at treating various diseases, including cancer, cardiovascular disorders, and neurological conditions. Its ability to form stable yet reactive intermediates makes it an indispensable building block in the pharmaceutical industry.
Another significant application of 4-Formyl-N-(2-(2-Methoxy-4-Methylphenoxy)ethyl)benzamide is in the field of organic light-emitting diodes (OLEDs). This material can be engineered to exhibit desirable photophysical properties, such as high fluorescence and stability, which are crucial for the efficiency and longevity of OLEDs. By incorporating this compound into OLED systems, manufacturers can enhance the performance of display and lighting technologies. Specifically, its methoxy and methylphenoxy groups contribute to tuning the electronic properties, making it a valuable component in the development of next-generation electronic displays.
4-Formyl-N-(2-(2-Methoxy-4-Methylphenoxy)ethyl)benzamide also finds application in the field of material science, particularly in the synthesis of advanced polymers. Its structural flexibility and reactivity allow it to be used as a monomer or a modifying agent in polymerization processes. These advanced polymers can be utilized in various high-performance materials, such as coatings, adhesives, and composite materials. The incorporation of this compound into polymer matrices can result in enhanced mechanical properties, thermal stability, and chemical resistance, making it highly valuable for the production of durable and high-performance materials.
In addition to its use in pharmaceuticals, electronics, and materials science, 4-Formyl-N-(2-(2-Methoxy-4-Methylphenoxy)ethyl)benzamide is also employed in agricultural chemistry. It serves as a key intermediate in the synthesis of agrochemicals, such as herbicides and pesticides. The specific molecular structure of this compound enables the development of chemicals that can effectively target and neutralize pests while minimizing harm to crops and the environment. Its role in enhancing the effectiveness and safety of agrochemical products underscores its importance in promoting sustainable agricultural practices and ensuring food security.
Catalog | Product Name | CAS | Inquiry |
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BADC-00517 | 4-Formyl-N-(2-Isopropoxyethyl)benzamide | 1061567-05-2 | |
BADC-00529 | 4-Formyl-N-(2-Phenoxyethyl)benzamide | 1225575-00-7 | |
BADC-00530 | 4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide | 1225587-15-4 | |
BADC-00537 | 4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide | 1225964-49-7 | |
BADC-00538 | 4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide | 1225964-74-8 | |
BADC-00544 | 4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide | 1226012-11-8 | |
BADC-00549 | 4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide | 1226076-16-9 | |
BADC-00550 | 4-Formyl-N-(2-(mesityloxy)ethyl)benzamide | 1226076-32-9 | |
BADC-00552 | 4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide | 1226105-58-3 | |
BADC-00554 | 4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide | 1226217-30-6 |
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