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Sku CI28453_100_G
Chem Impex
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Product Information

Product Name
6-Quinolinecarboxylic acid methyl ester
Brand Name
Chem Impex
Product Number
28453
CAS
38896-30-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
736812
IUPAC Name
methyl quinoline-6-carboxylate
InChI Key
XSRWQTDEIOHXSL-UHFFFAOYSA-N
SMILES
COC(=O)C1=CC2=C(C=C1)N=CC=C2

Application

6-Quinolinecarboxylic acid methyl ester is widely utilized in research focused on:

Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting infectious diseases and cancer. Its unique structure allows for the modification of biological activity.

Fluorescent Probes: It is employed in the development of fluorescent probes for biological imaging. The compound's ability to emit light under specific conditions makes it valuable in tracking cellular processes.

Ligand Development: In coordination chemistry, it acts as a ligand in metal complex formation. These complexes are crucial in catalysis and materials science, enhancing reaction efficiency and selectivity.

Research in Organic Chemistry: The compound is used in organic synthesis as a building block for creating more complex molecules, facilitating the exploration of new chemical reactions and pathways.

Antimicrobial Studies: Its application in antimicrobial research helps in the development of new agents against resistant strains of bacteria, addressing a significant challenge in modern medicine.

References

Oxidative Dehydrogenation of N-Heterocycles Promoted by N/P-Doped Carbon Materials

Publication Name: Synfacts
Publication Date: 2022-08-18
DOI: 10.1055/s-0041-1738293

Recent investigations into synthesis and pharmacological activities of phenoxy acetamide and its derivatives (chalcone, indole and quinoline) as possible therapeutic candidates

Publication Name: Journal of the Iranian Chemical Society
Publication Date: 2021-02-01
DOI: 10.1007/s13738-021-02172-5

In crystallo-screening for discovery of human norovirus 3C-like protease inhibitors

Publication Name: Journal of Structural Biology: X
Publication Date: 2020
DOI: 10.1016/j.yjsbx.2020.100031

Catalytic Arylation of a C-H Bond in Pyridine and Related Six-Membered N-Heteroarenes Using Organozinc Reagents

Publication Name: Chemistry – An Asian Journal
Publication Date: 2012-03-22
DOI: 10.1002/asia.201100971