4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide - CAS 1226105-58-3

4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide - CAS 1226105-58-3 Catalog number: BADC-00552

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

Category
ADCs Linker
Product Name
4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide
CAS
1226105-58-3
Catalog Number
BADC-00552
Molecular Formula
C17H17NO3
Molecular Weight
283.32
4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide

Ordering Information

Catalog Number Size Price Quantity
BADC-00552 -- $--
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Description
4-Formyl-N-(2-(o-tolyloxy)ethyl)benzamide is a linker for antibody-drug-conjugation (ADC).
IUPAC Name
4-formyl-N-[2-(2-methylphenoxy)ethyl]benzamide
Canonical SMILES
CC1=CC=CC=C1OCCNC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C17H17NO3/c1-13-4-2-3-5-16(13)21-11-10-18-17(20)15-8-6-14(12-19)7-9-15/h2-9,12H,10-11H2,1H3,(H,18,20)
InChIKey
AIRZOOGNCSIRBQ-UHFFFAOYSA-N
Shipping
Room temperature

4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide has potential applications in medicinal chemistry. The compound’s structural components suggest that it may act as a core scaffold in the development of new pharmaceuticals. The presence of the formyl and benzamide groups indicates potential interactions with biological targets such as enzymes or receptors. This capability allows for the modification of the compound to optimize its efficacy and selectivity in drug development, including anti-inflammatory, antimicrobial, or anticancer agents. The aromatic tolyloxy group adds to its ability to traverse lipid membranes, enhancing its applicability in drug delivery systems.

In the field of materials science, 4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide could be utilized in the synthesis of advanced polymers. The compound’s reactive formyl group can be used in polymerization reactions to create new polymeric materials with specialized properties such as thermal stability, mechanical strength, or chemical resistance. These polymers could find applications in high-performance materials for aerospace, automotive, or electronic industries. Additionally, its aromatic nature could contribute to electronic or optoelectronic properties, making it valuable in the development of conductive polymers and organic semiconductors.

4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide may also be used in the synthesis of organic intermediates in fine chemical manufacturing. The chemical structure allows for various functional group transformations, making it a versatile intermediate in the production of dyes, pigments, agrochemicals, and specialty chemicals. Its ability to undergo condensation reactions could lead to the formation of complex molecules required in these industries. The compound could serve as a building block for more intricate molecular architectures, enhancing product performance and expanding application possibilities.

In the realm of analytical chemistry, 4-Formyl-N-(2-(o-Tolyloxy)ethyl)benzamide could serve as a standard or reagent. Its defined structure and reactive sites can be utilized in various analytical techniques such as chromatography or spectroscopy to identify, quantify, or monitor chemical substances. The precise measurement of its chemical interactions can assist in the development of calibration standards, ensuring accuracy in analytical methods. Additionally, it could be used in the synthesis of labeled compounds for use in tracing studies or mechanistic investigations within complex biological or chemical systems.

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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