webinar
Oct. 27-28, 2025, Boston, MA, USA - Booth 114.
Read More

N-(2-(3,4-dimethylphenoxy)ethyl)-4-formylbenzamide

  CAS No.: 1226096-54-3   Cat No.: BADC-00551 4.5  

N-(2-(3,4-dimethylphenoxy)ethyl)-4-formylbenzamide serves as a reactive aldehyde ADC linker for stable and selective conjugation to antibodies, improving payload attachment and targeted delivery in ADC therapeutics.

N-(2-(3,4-dimethylphenoxy)ethyl)-4-formylbenzamide

Structure of 1226096-54-3

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C18H19NO3
Molecular Weight
297.35
Shipping
Room temperature, or blue ice upon request.

* For research and manufacturing use only. We do not sell to patients.

Size Price Stock Quantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

Popular Publications Citing BOC Sciences Products
IUPAC Name
N-[2-(3,4-dimethylphenoxy)ethyl]-4-formylbenzamide
Canonical SMILES
CC1=C(C=C(C=C1)OCCNC(=O)C2=CC=C(C=C2)C=O)C
InChI
InChI=1S/C18H19NO3/c1-13-3-8-17(11-14(13)2)22-10-9-19-18(21)16-6-4-15(12-20)5-7-16/h3-8,11-12H,9-10H2,1-2H3,(H,19,21)
InChIKey
PUESVCWYXHKETL-UHFFFAOYSA-N
Shipping
Room temperature, or blue ice upon request.

N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide is gaining recognition in the pharmaceutical field due to its potentially broad range of therapeutic applications. Its chemical structure, characterized by the dimethylphenoxy and formylbenzamide moieties, allows for diverse biological interactions which are crucial for its function as a therapeutic agent. This compound is being extensively studied for its potential role in addressing several chronic conditions, thereby contributing significantly to drug discovery and development processes. Its chemical attributes make it a valuable candidate for further exploration in medicinal chemistry.

One of the critical applications of N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide is in the development of novel analgesics. The compound's ability to modulate pain pathways makes it an attractive candidate for treating chronic pain conditions. By targeting specific receptors and enzymes implicated in pain transmission, it could offer a new mechanism of action distinct from traditional analgesics. This can be particularly beneficial in providing relief for patients who have not responded well to existing pain management therapies, as well as reducing the risk of dependency associated with opioid medications.

N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide is also being investigated for its anti-inflammatory properties. Its potential to interfere with inflammatory mediators suggests that it could be effective in managing autoimmune diseases such as lupus and psoriasis. By inhibiting the production or action of pro-inflammatory cytokines, this compound could reduce the excessive immune response characteristic of these disorders. Researchers are focused on understanding its mode of action through clinical and preclinical studies, hoping to provide a new avenue for treatment that is both effective and has fewer side effects.

Furthermore, the compound has shown potential in neuroprotective applications. In diseases such as Alzheimer's and Parkinson’s, N-(2-(3,4-Dimethylphenoxy)ethyl)-4-Formylbenzamide may help protect nerve cells from the detrimental processes that lead to neurodegeneration. The compound might offer a mechanism to mitigate or even reverse neuronal damage, providing hope for new treatment paradigms in managing neurodegenerative disorders. This aligns with the growing need for innovative therapies that can address the root causes of these diseases rather than just alleviating symptoms, thereby improving the quality of life for affected individuals.

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

Related Products

Contact our experts today for pricing and comprehensive details on our ADC offerings.

You May Also Be Interested In

From cytotoxin synthesis to linker design, discover our specialized services that complement your ADC projects.

ADC Linker Development Enzyme Cleavable Linker Cathepsin B Cleavable Linker/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker/Hydrazone Linker

Unlock Deeper ADC Insights

Learn more about payload design, linker strategies, and integrated CDMO support through our curated ADC content.

Linkers - A Crucial Factor in Antibody–Drug Conjugates In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress New Structural Insights Solve Instability Issues of Maleimide Linkers in ADCs PEG Linkers in Antibody-Drug Conjugates Peptide Linkers in Antibody-Drug Conjugates Disulfide Linkers in Antibody-Drug Conjugates Biotinylation Reagents in Antibody-Drug Conjugates Maleimide Linkers in Antibody-Drug Conjugates Current ADC Linker Chemistry SPDB Linkers in Antibody-Drug Conjugates

Explore More ADC Products

Find exactly what your project needs from our expanded range of ADCs, offering flexible options to fit your timelines and goals.

ADC Cytotoxin

Powerful Targeted Cancer Solutions

ADC  Cytotoxin with Linker

Enhanced Stability And Efficacy

ADC Linker

Precise Conjugation For Success

Antibody-Drug  Conjugates (ADCs)

Maximized Therapeutic Performance

Auristatins

Next-Level Tubulin Inhibition

Calicheamicins

High-Impact DNA Targeting

Camptothecins

Advanced Topoisomerase Inhibition

Daunorubicins / Doxorubicins

Trusted Anthracycline Payloads

Duocarmycins

Potent DNA Alkylation Agents

Maytansinoids

Superior Microtubule Disruption

Pyrrolobenzodiazepines

Ultra-Potent DNA Crosslinkers

Traditional Cytotoxic Agents

Proven Chemotherapy Solutions

Cleavable Linker

Precise Intracellular Drug Release

Non-Cleavable Linker

Exceptional Long-Term Stability

Historical Records: NHS-SS-Ph | MCC-Modified Daunorubicinol | Mc-MMAF | C-11 | 4-nitrophenyl 2-(pyridin-2-yldisulfanyl)ethyl carbonate | Daun02 | Dolastatin 10 | MA-PEG4-vc-PAB-DMEA-duocarmycin DM | Sacituzumab govitecan | N-(2-(3,4-dimethylphenoxy)ethyl)-4-formylbenzamide | 2,5-Dioxopyrrolidin-1-Yl 3-(2,4-Di-Tert-Pentylphenoxy)propanoate
Send Inquiry
Verification code
Inquiry Basket