4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide - CAS 1225964-49-7

4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide - CAS 1225964-49-7 Catalog number: BADC-00537

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

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide
CAS
1225964-49-7
Catalog Number
BADC-00537
Molecular Formula
C19H21NO3
Molecular Weight
311.37
4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00537 -- $--
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Description
4-Formyl-N-(2-(2-isopropylphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
4-formyl-N-[2-(2-propan-2-ylphenoxy)ethyl]benzamide
Canonical SMILES
CC(C)C1=CC=CC=C1OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C19H21NO3/c1-14(2)17-5-3-4-6-18(17)23-12-11-20-19(22)16-9-7-15(13-21)8-10-16/h3-10,13-14H,11-12H2,1-2H3,(H,20,22)
InChIKey
LIHPAAFLVLSEFH-UHFFFAOYSA-N
Shipping
Room temperature, or blue ice upon request.

Pharmaceutical Applications: One of the primary applications of 4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide lies in the pharmaceutical industry. This compound is valuable due to its potential as a precursor in the synthesis of biologically active molecules. It can be utilized in the creation of drugs that target specific cellular pathways or biochemical processes. The presence of the formyl group, along with the benzamide structure, allows for versatile chemical modifications, enabling researchers to investigate a wide range of therapeutic areas, including cancer, cardiovascular diseases, and neurological disorders. As a building block, it can contribute to the development of novel pharmaceuticals aimed at improving human health and alleviating various medical conditions.

Agricultural Chemistry: In the field of agriculture, 4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide serves as an essential intermediate in the synthesis of agrochemicals such as herbicides and fungicides. The compound’s structural features make it suitable for creating molecules that can protect crops from weeds, pests, and diseases, thereby enhancing agricultural productivity. Its effectiveness in forming derivatives with specific action mechanisms plays a crucial role in improving the yield and quality of crops. Additionally, the development of environmentally friendly agrochemicals is a growing concern, and compounds like 4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide contribute to this goal by offering pathways to new, less toxic agricultural products.

Material Science: The compound 4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide is also significant in material science, particularly in the design and synthesis of advanced polymers and resins. Its chemical structure allows it to participate in polymerization reactions, leading to the formation of materials with enhanced properties such as increased strength, flexibility, and resistance to environmental factors. These materials can be used in various industries, from packaging and textiles to automotive and aerospace engineering. The constant demand for new materials with superior performance characteristics drives ongoing research and development, wherein this compound plays a critical role.

Chemical Research and Development: Beyond its specific applications, 4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide is invaluable in chemical research and development. As a versatile intermediate, it is used in the synthesis of a wide array of chemical entities, providing a foundation for exploratory research into new chemical reactions and mechanisms. Researchers utilize this compound to develop new methodologies and protocols that can be applied across different branches of chemistry, including organic synthesis, medicinal chemistry, and analytical chemistry. Such advancements are crucial for the continual evolution of scientific knowledge and industrial innovation, and compounds like 4-Formyl-N-(2-(2-Isopropylphenoxy)ethyl)benzamide are at the heart of these progressive endeavors.

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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