4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide - CAS 1226218-43-4

4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide - CAS 1226218-43-4 Catalog number: BADC-00555

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4-Formyl-N-(2-(2, 3, 6-trimethylphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide
CAS
1226218-43-4
Catalog Number
BADC-00555
Molecular Formula
C19H21NO3
Molecular Weight
311.37
4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00555 -- $--
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Description
4-Formyl-N-(2-(2, 3, 6-trimethylphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
Canonical SMILES
CC1=C(C(=C(C=C1)C)OCCNC(=O)C2=CC=C(C=C2)C=O)C
InChI
InChI=1S/C19H21NO3/c1-13-4-5-14(2)18(15(13)3)23-11-10-20-19(22)17-8-6-16(12-21)7-9-17/h4-9,12H,10-11H2,1-3H3,(H,20,22)
InChIKey
LBTIJXJSOSDQMU-UHFFFAOYSA-N
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Room temperature

4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide, a synthetic compound, exhibits significant applications in the pharmaceutical industry, primarily as an intermediate in drug synthesis. Its structural versatility allows it to function as a vital building block in creating a variety of therapeutic agents. For instance, it’s utilized in the development of anti-inflammatory and analgesic medications, leveraging its ability to bind to specific biological targets and modulate inflammatory pathways. This application is crucial as it aids in the efficient production of vital medications that can manage pain and inflammation in chronic conditions.

Another important application of 4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide is in cancer research and treatment. The compound’s unique chemical properties enable it to interfere with the proliferation of cancer cells. By incorporating it into chemotherapy drugs, researchers can maximize the therapeutic efficacy while minimizing adverse side effects. Its role in oncology highlights its potential in advancing cancer treatments, providing hope for improved patient outcomes. This application underscores the compound’s importance in the continuous effort to develop more effective and targeted cancer therapies.

In the field of materials science, 4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide serves as a precursor for the synthesis of organic semiconductors and polymers. The electronic properties of these materials make them suitable for use in organic electronic devices such as organic light-emitting diodes (OLEDs), solar cells, and field-effect transistors. By contributing to the development of advanced materials with better performance and stability, this compound plays a crucial role in the innovation and improvement of electronic devices, which are integral to various industries and consumer electronics.

Lastly, 4-Formyl-N-(2-(2,3,6-Trimethylphenoxy)ethyl)benzamide is also employed in agricultural chemistry as part of the formulation of agrochemicals. It can be used in the synthesis of herbicides, pesticides, and growth regulators that help protect crops from pests and diseases while enhancing growth. This application is vital for ensuring food security and agricultural productivity, as it enables the creation of more effective and safer agricultural products. By protecting and promoting healthy crop growth, this compound helps sustain agricultural output and contributes to the global food supply chain.

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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