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Sku CI28478_5_G
Chem Impex
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Product Information

Product Name
2-Chloroquinoline-3-boronic acid
Brand Name
Chem Impex
Product Number
28478
CAS
128676-84-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
4198643
IUPAC Name
(2-chloroquinolin-3-yl)boronic acid
InChI Key
JAQXYUOPSOXQCG-UHFFFAOYSA-N
SMILES
B(C1=CC2=CC=CC=C2N=C1Cl)(O)O

Application

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

Pharmaceutical Development: This compound serves as a key building block in the synthesis of various pharmaceutical agents, particularly those targeting cancer and infectious diseases.

Organic Synthesis: It is employed in cross-coupling reactions, which are essential for creating complex organic molecules, making it valuable in the development of new materials and chemicals.

Bioconjugation: The unique properties of this boronic acid facilitate the attachment of biomolecules, enhancing drug delivery systems and improving the efficacy of therapeutic agents.

Fluorescent Probes: Researchers utilize this compound in the creation of fluorescent probes for biological imaging, allowing for real-time tracking of cellular processes.

Environmental Applications: It is also being explored for use in the detection and removal of pollutants, showcasing its potential in environmental chemistry and sustainability efforts.

References Data Source From Pubchem

Extending the Utility of the Bartoli Indolization: Synthesis of Marinoquinolines C and E

Publication Name: Synlett
Publication Date: 2013-01-23
DOI: 10.1055/s-0032-1318137

Quinolyllithium Compounds

Publication Name: Science of Synthesis
Publication Date: 2006

Substitution of Metalated Quinolines

Publication Name: Science of Synthesis
Publication Date: 2005