N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide - CAS 1225790-59-9

N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide - CAS 1225790-59-9 Catalog number: BADC-00535

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N-(2-(4-Ethylphenoxy)ethyl)-4-formylbenzamide is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide
CAS
1225790-59-9
Catalog Number
BADC-00535
Molecular Formula
C18H19NO3
Molecular Weight
297.35
N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00535 -- $-- Inquiry
Description
N-(2-(4-Ethylphenoxy)ethyl)-4-formylbenzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
N-[2-(4-ethylphenoxy)ethyl]-4-formylbenzamide
Canonical SMILES
CCC1=CC=C(C=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C18H19NO3/c1-2-14-5-9-17(10-6-14)22-12-11-19-18(21)16-7-3-15(13-20)4-8-16/h3-10,13H,2,11-12H2,1H3,(H,19,21)
InChIKey
SUQFQPNXVBVFJH-UHFFFAOYSA-N
Shipping
Room temperature, or blue ice upon request.

N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide is an emerging compound of interest in the domain of drug development and medicinal chemistry. The structure of this molecule, with an ethylphenoxy group linked to a formylbenzamide framework, suggests its potential to interact beneficially with biological systems. This configuration boosts its utility as a prototype compound in the search for new anti-inflammatory agents. Given the ongoing research into substances that can effectively manage inflammation with fewer side effects, N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide offers a promising template. It might interact with key enzymes or receptors that regulate inflammatory processes, potentially leading to new treatments for conditions such as arthritis and asthma.

In addition to its pharmaceutical prospects, N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide shows promise as a versatile building block in the synthesis of more complex organic compounds. The ethylphenoxy group enhances the compound’s solubility and stability, making it an excellent candidate for further chemical modification. Researchers can explore its reactivity in various synthetic pathways, which might include conjugate additions or cyclization reactions, to create novel compounds with enhanced or targeted biological activity. This adaptability is particularly beneficial in the lead optimization phase of drug development, allowing for the fine-tuning of pharmacodynamic and pharmacokinetic properties to enhance therapeutic efficacy.

The compound also has potential applications in developing advanced agricultural products. With its ability to be chemically modified, N-(2-(4-Ethylphenoxy)ethyl)-4-Formylbenzamide could serve as a precursor to new agrochemicals, such as herbicides or pesticides, that offer improved specificity and environmental profiles. The unique characteristics imparted by the ethylphenoxy moiety may positively influence its action against agricultural pests or weeds, reducing non-target impacts. This application not only supports crop health but also aligns with global movements towards sustainable agriculture by offering alternatives with potentially lower ecological footprints.

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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