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Sku CI28965_25_G
Chem Impex
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Product Information

Product Name
2-Methoxypyridine-3-boronic acid
Brand Name
Chem Impex
Product Number
28965
CAS
163105-90-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2762709
IUPAC Name
(2-methoxy-3-pyridinyl)boronic acid
InChI Key
NVOLYUXUHWBCRJ-UHFFFAOYSA-N
SMILES
B(C1=C(N=CC=C1)OC)(O)O

Description

2-Methoxypyridine-3-boronic acid is widely utilized in research focused on:

Synthetic Chemistry: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.

Catalysis: It is employed as a ligand in palladium-catalyzed cross-coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis, enhancing reaction efficiency and selectivity.

Bioconjugation: The boronic acid functional group allows for selective binding to diols, making it useful in bioconjugation techniques for drug delivery systems and targeted therapies.

Material Science: It is used in the development of advanced materials, including sensors and polymers, due to its ability to form stable complexes with various substrates.

Analytical Chemistry: This compound can be utilized in the development of analytical methods for detecting and quantifying certain biomolecules, providing a reliable tool for researchers in biochemistry.

References Data Source From Pubchem

Suzuki Cross Coupling of Oligonucleotide Chlorobenzoic Acid Derivatives

Publication Name: Science of Synthesis
Publication Date: 2024

Cross Coupling of 3-Chloro-1H-2-benzopyran-1-one

Publication Name: Science of Synthesis
Publication Date: 2020

From a Pyridylboronic Acid and Di-tert-butyl Azodicarboxylate

Publication Name: Science of Synthesis
Publication Date: 2016

First Identification of Boronic Species as Novel Potential Inhibitors of the Staphylococcus aureus NorA Efflux Pump

Publication Name: Journal of Medicinal Chemistry
Publication Date: 2014-02-19
DOI: 10.1021/jm401808n