N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide - CAS 1225705-45-2

N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide - CAS 1225705-45-2 Catalog number: BADC-00533

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

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

Category
ADCs Linker
Product Name
N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide
CAS
1225705-45-2
Catalog Number
BADC-00533
Molecular Formula
C16H14FNO3
Molecular Weight
287.29
N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00533 -- $-- Inquiry
Description
N-(2-(2-Fluorophenoxy)ethyl)-4-formylbenzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
N-[2-(2-fluorophenoxy)ethyl]-4-formylbenzamide
Canonical SMILES
C1=CC=C(C(=C1)OCCNC(=O)C2=CC=C(C=C2)C=O)F
InChI
InChI=1S/C16H14FNO3/c17-14-3-1-2-4-15(14)21-10-9-18-16(20)13-7-5-12(11-19)6-8-13/h1-8,11H,9-10H2,(H,18,20)
InChIKey
KVKGNWNKUGUSFR-UHFFFAOYSA-N
Shipping
Room temperature

N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide, a compound of notable interest, has been increasingly explored for its potential applications in the pharmaceutical industry. This chemical entity is often examined in the context of drug development due to its structural features, which may facilitate interactions with specific biological targets. The presence of the formyl group alongside the fluoro-substituted phenoxy moiety suggests potential utility in the synthesis of bioactive molecules, where modifications in such structures can lead to variations in activity or selectivity against certain biological pathways. Through these studies, researchers aim to uncover new therapeutic avenues, especially in challenging diseases that require more effective intervention strategies.

Furthermore, the compound's ability to influence interactions at the molecular level makes it an attractive candidate in medicinal chemistry research. Scientists focus on the compound’s role as a building block in constructing novel pharmacophores, which are parts of molecules responsible for their biological activity. By tweaking its structure, researchers can systematically evaluate changes in biological activity, offering insights into the relationships between chemical structure and biological function. This is particularly valuable in designing selective agents that can modulate specific proteins or enzymes implicated in disease processes, thereby advancing the development of more precise and targeted therapies.

In the realm of chemical biology, N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide might also serve as a probe or a scaffold for designing analytical tools. Its structural attributes allow it to be incorporated into larger molecular frameworks that can be used to explore complex biological environments. Such tools are essential for visualizing cellular processes or for identifying and validating new biological targets. Consequently, this enhances our understanding of cellular pathways and mechanisms at a molecular level, enabling researchers to devise better strategies for diagnostic or therapeutic purposes.

Lastly, the compound's versatile chemistry allows it to be utilized in a variety of synthetic methodologies, expanding its applicability beyond pharmaceuticals into fields such as materials science. Incorporating this compound into polymers or advanced materials could impart novel properties, potentially leading to innovative applications in electronics, coatings, or biocompatible materials. The ability to blend function with form is a driving force in material innovation, and N-(2-(2-Fluorophenoxy)ethyl)-4-Formylbenzamide presents exciting possibilities in this aspect, inviting multidisciplinary research efforts aimed at harnessing its full potential.

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

Why Choose BOC Sciences?

Customer Support

Providing excellent 24/7 customer service and support

Project Management

Offering 100% high-quality services at all stages

Quality Assurance

Ensuring the quality and reliability of products or services

Global Delivery

Ensuring timely delivery of products worldwide

Questions & Comments
Verification code
Send Inquiry
Verification code
Resources & Supports
Inquiry Basket