4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide - CAS 1226217-30-6

4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide - CAS 1226217-30-6 Catalog number: BADC-00554

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

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

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide
CAS
1226217-30-6
Catalog Number
BADC-00554
Molecular Formula
C19H21NO3
Molecular Weight
311.37
4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00554 -- $--
Inquiry
Description
4-Formyl-N-(2-(4-isopropylphenoxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
4-formyl-N-[2-(4-propan-2-ylphenoxy)ethyl]benzamide
Canonical SMILES
CC(C)C1=CC=C(C=C1)OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C19H21NO3/c1-14(2)16-7-9-18(10-8-16)23-12-11-20-19(22)17-5-3-15(13-21)4-6-17/h3-10,13-14H,11-12H2,1-2H3,(H,20,22)
InChIKey
ZPRLTBCFAFQUAX-UHFFFAOYSA-N
Shipping
Room temperature

4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide, often referred to by its chemical structure, has garnered attention in various fields of research and industry due to its unique properties. One of its primary applications is in the realm of pharmaceuticals. Being a benzamide derivative, it has been explored for its potential as an intermediate in the synthesis of drug compounds. Researchers have utilized this compound in trials to develop new therapeutic agents aimed at treating various ailments, such as inflammation and infections. The compound’s specific structure allows it to act as a crucial building block, influencing the pharmacokinetic and pharmacodynamic properties of the resultant drug, thus enhancing its efficacy and safety profile.

Another significant application of 4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide lies in the agrochemical industry. Due to its potential biological activity, it has been investigated for use in the development of new pesticides and herbicides. The compound’s ability to interfere with specific biological pathways in pests and weeds allows for the formulation of effective agrochemical solutions that are essential for sustainable agriculture. Its properties contribute to the control of pests that are resistant to traditional pesticides, thereby playing a crucial role in ensuring crop protection and food security.

In addition to its pharmaceutical and agrochemical applications, 4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide is also noted for its use in the field of materials science. Specifically, it is explored for its potential role in the development of functionalized polymers and advanced materials. The compound’s formyl and benzamide groups can participate in various chemical reactions, making it a versatile intermediate in polymer synthesis. These polymers could have applications in creating high-performance materials that are used in a variety of industries, including automotive, aerospace, and consumer electronics. Such materials may demonstrate superior mechanical, thermal, and chemical resistance properties.

Lastly, the compound has been identified as a valuable tool in chemical research and development. In synthetic organic chemistry, 4-Formyl-N-(2-(4-Isopropylphenoxy)ethyl)benzamide serves as a key reagent in forming carbon-nitrogen bonds, which are fundamental in creating complex organic molecules. This has implications for the synthesis of novel compounds in the laboratory setting. Researchers leverage its stable structure and reactivity to develop new synthetic methodologies, contributing to advancements in the understanding and manipulation of chemical reactions. Its role as a reagent underscores the importance of such compounds in driving innovation and discovery in the field of chemistry.

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
Inquiry Basket