4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide - CAS 1226324-22-6

4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide - CAS 1226324-22-6 Catalog number: BADC-00560

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

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide
CAS
1226324-22-6
Catalog Number
BADC-00560
Molecular Formula
C17H17NO4
Molecular Weight
299.32
4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00560 -- $--
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Description
4-Formyl-N-(2-(3-methoxyphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
4-formyl-N-[2-(3-methoxyphenoxy)ethyl]benzamide
Canonical SMILES
COC1=CC(=CC=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C17H17NO4/c1-21-15-3-2-4-16(11-15)22-10-9-18-17(20)14-7-5-13(12-19)6-8-14/h2-8,11-12H,9-10H2,1H3,(H,18,20)
InChIKey
VQHKFOJUFDMPRQ-UHFFFAOYSA-N
Shipping
-20°C (International: -20°C)

One of the principal applications of 4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide lies in the field of medicinal chemistry. This compound exhibits unique pharmacological properties that make it a potential candidate for drug development, particularly as an inhibitor in various enzymatic pathways. Its structural features allow it to interact effectively with biological targets, potentially offering therapeutic benefits in the treatment of inflammatory diseases, cancer, or other ailments where selective enzyme modulation is crucial. Consequently, extensive research and development efforts are geared toward exploring its efficacy and safety as a lead compound in drug discovery programs.

In addition to its application in medicinal chemistry, 4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide is also valuable in biochemical research. It serves as a useful tool for studying enzyme kinetics and binding interactions, providing insights into the mechanistic aspects of enzyme regulation and inhibition. Researchers utilize this compound to elucidate the molecular underpinnings of enzyme functions, which can have broader implications for understanding biological processes and developing novel therapeutic strategies. By serving as a model compound in experimental setups, it helps advance the field of biochemical research and enhances our understanding of complex biological systems.

Another significant application of 4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide is in the realm of chemical synthesis. Given its unique aldehyde and amide functional groups, this compound is used as an intermediate in the synthesis of more complex molecules. These functional groups facilitate various chemical reactions such as nucleophilic addition, condensation, and cyclization, enabling the synthesis of diverse chemical entities. Synthetic chemists leverage this compound to create new molecular frameworks, which can be further explored for their chemical and biological properties. This makes it an indispensable tool in both academic research and industrial applications where novel compound libraries are generated.

Finally, 4-Formyl-N-(2-(3-Methoxyphenoxy)ethyl)benzamide finds application in material science, particularly in the design and development of novel materials. Its ability to form stable complexes with metals and its functional versatility makes it suitable for creating advanced materials with specific properties. These materials can be employed in various technological applications such as catalysis, electronic devices, and sensors. Researchers are continually exploring new ways to incorporate this compound into material matrices to enhance performance characteristics and develop innovative solutions for industrial challenges. Its contribution to material science underscores its multifaceted utility and potential for future technological advancements.

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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