4-formylphenyl 3-iodo-4-methoxybenzoate - CAS 875107-50-9

4-formylphenyl 3-iodo-4-methoxybenzoate - CAS 875107-50-9 Catalog number: BADC-00701

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4-formylphenyl 3-iodo-4-methoxybenzoate is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
4-formylphenyl 3-iodo-4-methoxybenzoate
CAS
875107-50-9
Catalog Number
BADC-00701
Molecular Formula
C15H11IO4
Molecular Weight
382.15
4-formylphenyl 3-iodo-4-methoxybenzoate

Ordering Information

Catalog Number Size Price Quantity
BADC-00701 -- $--
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Description
4-formylphenyl 3-iodo-4-methoxybenzoate is a linker for antibody-drug-conjugation (ADC).
Canonical SMILES
COC1=C(C=C(C=C1)C(=O)OC2=CC=C(C=C2)C=O)I
InChI
InChI=1S/C15H11IO4/c1-19-14-7-4-11(8-13(14)16)15(18)20-12-5-2-10(9-17)3-6-12/h2-9H,1H3
InChIKey
KSLMVQZBBARVRI-UHFFFAOYSA-N
Shipping
Room temperature

4-formylphenyl 3-iodo-4-methoxybenzoate, a versatile synthetic chemical compound, holds immense potential for a multitude of scientific research and drug development applications. Here are four key applications highlighted with a high degree of perplexity and burstiness:

Organic Synthesis: Embraced as a pivotal intermediate in synthesizing intricate organic compounds, 4-formylphenyl 3-iodo-4-methoxybenzoate serves as a fundamental building block in crafting diverse heterocyclic molecules essential in medicinal chemistry. Researchers harness its potential to innovate new pharmaceuticals and bioactive molecules with a myriad of therapeutic properties, pushing the boundaries of molecular innovation.

Chemical Biology: Encompassing the realm of chemical biology, this compound emerges as a potent tool for probing biological processes at the molecular scale. Its reactive functional groups enable the establishment of covalent bonds with biological macromolecules, empowering researchers to tag and monitor specific proteins or nucleic acids. This methodology aids in unveiling the intricate mechanisms of drug action and protein interactions within cellular environments, paving the way for groundbreaking discoveries.

Material Science: Within the domain of material science, 4-formylphenyl 3-iodo-4-methoxybenzoate finds its niche in advancing materials technology, especially in the realm of polymer and nanomaterial development. By integrating functional groups into polymer chains, this compound enhances material properties such as adhesion, conductivity, or biocompatibility, driving innovation in biomedical device fabrication, sensor technology, and electronic applications, propelling materials science into new frontiers.

Medicinal Chemistry: Playing a pivotal role in drug discovery endeavors, this compound acts as a crucial precursor for synthesizing bioactive molecules and pharmacophores. Its structural adaptability allows for the creation of a myriad of derivatives with the potential for therapeutic efficacy. Through strategic structural modifications, researchers can fine-tune the efficacy and specificity of drug candidates, tailoring them to target precise biological pathways or diseases, heralding a new era in precision medicine.

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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