4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide - CAS 1226076-16-9

4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide - CAS 1226076-16-9 Catalog number: BADC-00549

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

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide
CAS
1226076-16-9
Catalog Number
BADC-00549
Molecular Formula
C19H21NO3
Molecular Weight
311.37
4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00549 -- $-- Inquiry
Description
4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
4-formyl-N-[2-(3-propan-2-ylphenoxy)ethyl]benzamide
Canonical SMILES
CC(C)C1=CC(=CC=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C19H21NO3/c1-14(2)17-4-3-5-18(12-17)23-11-10-20-19(22)16-8-6-15(13-21)7-9-16/h3-9,12-14H,10-11H2,1-2H3,(H,20,22)
InChIKey
KVAKSRMJLXMVJX-UHFFFAOYSA-N
Shipping
Room temperature, or blue ice upon request.

4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide, a synthetic organic compound, has found substantial applications in medicinal chemistry, particularly in the design and development of novel therapeutic agents. Research has demonstrated its potential as a lead compound in the development of anti-cancer drugs. Studies have shown that this compound exhibits significant cytotoxic activity against various cancer cell lines, inhibiting their growth and proliferation. Its unique chemical structure allows for the modification and optimization to enhance its pharmacological properties, making it a promising candidate in oncology drug development. Additionally, the compound’s ability to induce apoptosis in cancer cells through specific signaling pathways further underscores its potential in targeted cancer therapy.

Another notable application of 4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide is in the field of neuropharmacology. The compound has been explored for its neuroprotective properties, particularly in the context of neurodegenerative diseases such as Alzheimer’s and Parkinson’s. Preclinical studies have indicated that it can cross the blood-brain barrier and exert protective effects on neuronal cells. This is achieved through its antioxidant properties and its ability to modulate neuroinflammatory pathways. The compound’s mechanism of action involves the inhibition of key enzymes and receptors that are implicated in the pathogenesis of neurodegenerative conditions, offering a potential therapeutic avenue for patients suffering from these debilitating diseases.

In addition to its medicinal applications, 4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide has shown promise in agricultural sciences, particularly as a bioactive agent in pest management. Its efficacy as a biopesticide is attributed to its ability to interfere with the reproductive and developmental processes of various insect pests. The compound acts as an insect growth regulator, disrupting the normal growth patterns and leading to decreased pest populations. This environmentally friendly approach to pest control not only reduces the reliance on conventional chemical pesticides, which are often associated with adverse environmental and health effects, but also supports sustainable agricultural practices.

Finally, 4-Formyl-N-(2-(3-isopropylphenoxy)ethyl)benzamide has potential applications in materials science, specifically in the development of advanced polymers and coatings. Its unique structural properties facilitate its incorporation into polymer matrices, leading to enhanced material performance characteristics such as increased thermal stability, mechanical strength, and resistance to chemical degradation. This makes it an attractive candidate for use in high-performance materials that are employed in various industrial applications, including automotive, aerospace, and electronics. The ability to tailor the chemical structure of this compound further allows for the customization of polymer properties to meet specific application requirements, opening up new possibilities in material innovation.

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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