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N-(2-(3-(Dimethylamino)phenoxy)ethyl)-4-Formylbenzamide

  CAS No.: 1226019-77-7   Cat No.: BADC-00545 4.5  

N-(2-(3-(Dimethylamino)phenoxy)ethyl)-4-Formylbenzamide is an aldehyde-bearing ADC linker that enables efficient antibody conjugation and enhances payload stability. Its dimethylamino group contributes to improved pharmacokinetics in antibody-drug conjugates.

N-(2-(3-(Dimethylamino)phenoxy)ethyl)-4-Formylbenzamide

Structure of 1226019-77-7

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ADC Linker
Molecular Formula
C18H20N2O3
Molecular Weight
312.36
Shipping
Room temperature

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Canonical SMILES
CN(C)C1=CC(=CC=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C18H20N2O3/c1-20(2)16-4-3-5-17(12-16)23-11-10-19-18(22)15-8-6-14(13-21)7-9-15/h3-9,12-13H,10-11H2,1-2H3,(H,19,22)
InChIKey
PAUHDWYVMLPUPD-UHFFFAOYSA-N
Shipping
Room temperature

N-(2-(3-(Dimethylamino)phenoxy)ethyl)-4-Formylbenzamide is a versatile chemical compound primarily used in the field of medicinal chemistry. Its unique structure allows it to interact with biological systems in a way that can be harnessed for therapeutic applications. In particular, the compound's ability to modulate the activity of various enzymes makes it a promising candidate for drug development. Researchers focus on its potential as a lead compound in the creation of new medications aimed at treating cancer, inflammation, and neurological disorders. The specificity with which this chemical can be tailored to interact with target proteins underlines its importance in the design of selective drugs that minimize side effects.

In addition to its role in drug development, N-(2-(3-(Dimethylamino)phenoxy)ethyl)-4-Formylbenzamide is also being explored for its applications in biochemical research. Its ability to bind with high affinity to certain enzymes makes it suitable for use as a molecular probe. This allows researchers to study the enzyme's function and structure in greater detail, providing insights that are critical for understanding complex biological processes. Moreover, its structural components enable modifications that can be used to visualize these enzymes within a living cell, offering valuable data on cellular mechanisms and potential intervention points for future therapeutic treatments.

Another key application of N-(2-(3-(Dimethylamino)phenoxy)ethyl)-4-Formylbenzamide is in the field of materials science. Its stable and reactive form allows it to be used as a building block in the synthesis of advanced polymers and materials with desired mechanical, thermal, or electrical properties. For instance, it can be incorporated into polymeric matrices to enhance durability, flexibility, or conductivity, making it ideal for use in electronics or structural components. The versatility of such modifications is beneficial in designing materials that require specific properties for specialized applications, such as in aerospace or medical devices.

Furthermore, the compound finds its application in analytical chemistry as a standard or reagent. Its precise and predictable reactions enable it to be used in the calibration of analytical instruments, contributing to the accuracy and reliability of quantitative analyses. Laboratories use it in various assays to detect or quantify other substances, taking advantage of its stability and reactivity. As a result, it plays a crucial role in ensuring the quality control of products, ranging from pharmaceuticals to food items, thereby safeguarding public health and compliance with regulatory standards.

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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