4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide - CAS 1225587-15-4

4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide - CAS 1225587-15-4 Catalog number: BADC-00530

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

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide
CAS
1225587-15-4
Catalog Number
BADC-00530
Molecular Formula
C17H17NO3
Molecular Weight
283.32
4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00530 -- $--
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Description
4-Formyl-N-(2-(m-tolyloxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
4-formyl-N-[2-(3-methylphenoxy)ethyl]benzamide
Canonical SMILES
CC1=CC(=CC=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C17H17NO3/c1-13-3-2-4-16(11-13)21-10-9-18-17(20)15-7-5-14(12-19)6-8-15/h2-8,11-12H,9-10H2,1H3,(H,18,20)
InChIKey
PGSTTXBZVVGQRP-UHFFFAOYSA-N
Shipping
Room temperature

4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide, a novel organic compound, serves as a significant intermediary in the synthesis of pharmaceutical agents. This compound’s unique structure makes it invaluable in the creation of drugs targeting various medical conditions. Its formyl group enables the formation of Schiff bases, which are crucial intermediates in the synthesis of various pharmaceutical agents. Additionally, it can be utilized in the development of molecules that inhibit specific enzymes, providing therapeutic benefits for conditions such as cancer and diabetes. Leveraging its distinct attributes, researchers can derive potent pharmaceutical candidates, underscoring its critical role in medicinal chemistry.

Another crucial application of 4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide is in the realm of organic synthesis, particularly in the production of complex organic molecules. Its ability to undergo various chemical reactions makes it an excellent building block for the synthesis of heterocyclic compounds, which are prevalent in many natural products and biologically active molecules. By facilitating the construction of diverse chemical structures, it aids in the development of new materials and chemicals for industrial purposes. This versatility highlights its importance in organic manufacturing processes, contributing to advancements in chemical production technologies.

In the field of material science, 4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide has shown potential in the development of advanced polymeric materials. The compound’s reactive formyl and amide groups allow it to initiate polymerization processes, leading to the formation of novel polymers with unique properties. These polymers can be used in various applications, ranging from electronics to biomedical devices owing to their enhanced stability and functionality. Thus, it plays a pivotal role in the innovation of high-performance materials, driving progress in material science and engineering.

The biochemical research domain also benefits from the application of 4-Formyl-N-(2-(m-Tolyloxy)ethyl)benzamide, particularly in enzyme studies and protein-ligand interactions. The compound’s structural elements make it a valuable probe for studying the binding mechanisms of enzymes and proteins. By examining how this compound interacts with biological molecules, scientists can gain insights into the fundamental processes of life and disease. This knowledge is crucial for the design of new drugs and therapeutic agents, making it an indispensable tool in biochemical and pharmaceutical research.

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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