4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide - CAS 1226012-11-8

4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide - CAS 1226012-11-8 Catalog number: BADC-00544

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4-Formyl-N-(2-(4-methoxyphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide
CAS
1226012-11-8
Catalog Number
BADC-00544
Molecular Formula
C17H17NO4
Molecular Weight
299.32
4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00544 -- $--
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Description
4-Formyl-N-(2-(4-methoxyphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
4-formyl-N-[2-(4-methoxyphenoxy)ethyl]benzamide
Canonical SMILES
COC1=CC=C(C=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C17H17NO4/c1-21-15-6-8-16(9-7-15)22-11-10-18-17(20)14-4-2-13(12-19)3-5-14/h2-9,12H,10-11H2,1H3,(H,18,20)
InChIKey
OBJVBNNTHREGJS-UHFFFAOYSA-N
Shipping
Room temperature

4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide, a versatile organic compound, plays a significant role in the field of medicinal chemistry. One key application is in the design and synthesis of potential anti-cancer agents. The compound’s unique chemical structure allows it to interact with various biological pathways associated with cancer cell proliferation. Researchers have been investigating its potential to inhibit specific enzymes that are crucial for the growth of cancer cells. By targeting these enzymes, 4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide can help in developing novel treatments that are both effective and have fewer side effects compared to traditional chemotherapy.

Another critical application of 4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide is in the development of anti-inflammatory drugs. Chronic inflammation is a significant underlying factor in many diseases, including arthritis, cardiovascular diseases, and autoimmune disorders. The compound’s ability to modulate inflammatory pathways offers a promising approach to creating new medications that can effectively reduce inflammation without the severe side effects often associated with current anti-inflammatory drugs. Researchers are focusing on how this compound can be optimized to enhance its efficacy and safety profile for long-term use in patients suffering from chronic inflammatory conditions.

In the realm of material science, 4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide serves as an important building block for the synthesis of advanced polymers and materials. These materials have applications in various industries, including electronics, optics, and coatings. The compound’s structural properties contribute to the development of polymers with unique characteristics, such as enhanced thermal stability, mechanical strength, and electrical conductivity. By integrating this compound into polymer matrices, scientists can design materials that meet the stringent requirements of high-performance applications, opening new possibilities for innovation in material science.

Lastly, 4-Formyl-N-(2-(4-Methoxyphenoxy)ethyl)benzamide is utilized in the field of organic electronics. Organic electronics, which include organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic solar cells (OSCs), benefit from the compound’s electronic properties. Its ability to act as a semiconductor or a charge transport material makes it a valuable component in the development of flexible, lightweight, and cost-effective electronic devices. Ongoing research aims to optimize the electronic properties of this compound to improve the performance and efficiency of organic electronic devices, contributing to the advancement of cutting-edge technologies in consumer electronics and renewable energy.

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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