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4-Formyl-N-(2-(p-Tolyloxy)ethyl)benzamide

  CAS No.: 1226279-82-8   Cat No.: BADC-00557 4.5  

4-Formyl-N-(2-(p-Tolyloxy)ethyl)benzamide is an aldehyde-based ADC linker that supports site-specific antibody conjugation and improves targeted payload release for enhanced ADC performance.

4-Formyl-N-(2-(p-Tolyloxy)ethyl)benzamide

Structure of 1226279-82-8

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ADC Linker
Molecular Formula
C17H17NO3
Molecular Weight
283.32
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Room temperature, or blue ice upon request.

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IUPAC Name
4-formyl-N-[2-(4-methylphenoxy)ethyl]benzamide
Canonical SMILES
CC1=CC=C(C=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C17H17NO3/c1-13-2-8-16(9-3-13)21-11-10-18-17(20)15-6-4-14(12-19)5-7-15/h2-9,12H,10-11H2,1H3,(H,18,20)
InChIKey
FSMWWWYTVKPGOP-UHFFFAOYSA-N
Shipping
Room temperature, or blue ice upon request.

4-Formyl-N-(2-(p-Tolyloxy)ethyl)benzamide, as an organic compound, has garnered significant interest for its multifaceted applications in the field of pharmaceuticals. One of its critical uses is as a building block in the synthesis of complex drug molecules. The unique structure of this compound allows it to participate in various chemical reactions, making it invaluable for chemists working to develop new therapeutic agents. Its ability to form stable intermediates makes it particularly useful in creating drugs aimed at treating ailments such as cancer and infectious diseases. The compound’s versatility in synthetic chemistry underscores its importance in the continuous search for innovative medical treatments.

In the realm of material science, 4-Formyl-N-(2-(p-Tolyloxy)ethyl)benzamide has found applications in the development of advanced polymeric materials. The compound’s functional groups allow for easy incorporation into polymer chains, resulting in materials with enhanced properties such as improved thermal stability and mechanical strength. These advanced polymers are crucial in various industries, including automotive, aerospace, and electronics, where materials that can withstand extreme conditions are essential. The role of this compound in producing high-performance materials demonstrates its potential in driving forward technological advancements and enhancing the longevity and reliability of numerous products.

The agrochemical industry has also leveraged the properties of 4-Formyl-N-(2-(p-Tolyloxy)ethyl)benzamide for the synthesis of novel agrochemicals. The compound serves as a precursor in the creation of pesticides and herbicides that are more effective and environmentally friendly. Its ability to be modified into various active molecules helps in combating pest resistance and promoting sustainable agriculture practices. By contributing to the development of safer and more efficient agrochemicals, this compound supports efforts to increase agricultural productivity while minimizing the ecological footprint. Its role in the agrochemical sector underscores its importance in addressing global food security challenges.

Moreover, 4-Formyl-N-(2-(p-Tolyloxy)ethyl)benzamide is utilized in the field of organic electronics, particularly in the synthesis of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound’s electronic properties make it suitable for use in these applications, where it contributes to the efficiency and performance of organic electronic devices. Its incorporation into OLEDs helps in producing displays with better brightness and energy efficiency, while in OPVs, it aids in the development of more efficient solar cells. The continuous improvement and miniaturization of electronic devices heavily rely on such compounds, highlighting its significance in the ever-evolving electronics industry.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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