4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide - CAS 1225964-74-8

4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide - CAS 1225964-74-8 Catalog number: BADC-00538

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4-Formyl-N-(2-(2, 4, 5-trimethylphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide
CAS
1225964-74-8
Catalog Number
BADC-00538
Molecular Formula
C19H21NO3
Molecular Weight
311.37
4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00538 -- $--
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Description
4-Formyl-N-(2-(2, 4, 5-trimethylphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
Canonical SMILES
CC1=CC(=C(C=C1C)OCCNC(=O)C2=CC=C(C=C2)C=O)C
InChI
InChI=1S/C19H21NO3/c1-13-10-15(3)18(11-14(13)2)23-9-8-20-19(22)17-6-4-16(12-21)5-7-17/h4-7,10-12H,8-9H2,1-3H3,(H,20,22)
InChIKey
HNXTXQVBTMASEB-UHFFFAOYSA-N
Shipping
-20°C (International: -20°C)

4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide, a versatile organic compound, finds key applications in medicinal chemistry. Its primary application is in the synthesis of pharmaceutical intermediates and active pharmaceutical ingredients (APIs). The compound’s unique chemical structure allows it to act as a crucial building block in drug discovery and development. It is frequently used in the creation of molecules with potential therapeutic benefits owing to its ability to interact with various biological targets. This makes it invaluable for developing new treatments for conditions such as cancer, inflammation, and infectious diseases, thereby contributing significantly to modern medicine.

Another significant application of 4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide lies in agrochemical research and development. The compound’s properties make it an ideal candidate for synthesizing new herbicides, insecticides, and fungicides that can improve crop yields and pest resistance. By incorporating 4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide into agrochemical formulations, researchers can create more effective and environmentally friendly products. These innovations are crucial for addressing global food security issues and supporting sustainable agricultural practices. This compound’s versatile chemistry thus plays a pivotal role in safeguarding crop health and productivity.

In the realm of materials science, 4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide is vital for developing new polymers and advanced materials. Its unique structural features facilitate the synthesis of high-performance materials with desirable properties such as enhanced strength, durability, and thermal stability. These materials can be utilized in a variety of industries, including automotive, aerospace, and electronics, where they contribute to the creation of more efficient and resilient products. The compound’s application in this field underscores its importance in advancing technology and enhancing material capabilities.

Finally, 4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide is also employed in the field of analytical chemistry as a reagent for various chemical analyses. Its reactivity and stability make it suitable for use in chromatographic and spectroscopic methods that ascertain the composition and purity of complex mixtures. This application is particularly valuable in quality control and research laboratories, where precise and accurate analysis is paramount. The role of this compound in analytical procedures ensures that products meet stringent standards and regulations, further highlighting its significance across diverse scientific disciplines.

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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