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Sku CI25061_5_G
Chem Impex
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Product Information

Product Name
Ethyl 6-chloro-4-hydroxyquinoline-3-carboxylate
Brand Name
Chem Impex
Product Number
25061
CAS
70271-77-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
718113
IUPAC Name
ethyl 6-chloro-4-oxo-1H-quinoline-3-carboxylate
InChI Key
ABZXBXREXPKTCN-UHFFFAOYSA-N
SMILES
CCOC(=O)C1=CNC2=C(C1=O)C=C(C=C2)Cl

Application

Ethyl 6-chloro-4-hydroxyquinoline-3-carboxylate is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting bacterial infections, due to its antibacterial properties.

Agricultural Chemicals: It is used in the formulation of agrochemicals, helping to develop effective pesticides and herbicides that enhance crop protection against pests and diseases.

Biochemical Research: Researchers employ this compound in studies related to enzyme inhibition and receptor binding, aiding in the understanding of biochemical pathways and drug interactions.

Material Science: The compound is explored for its potential applications in creating novel materials, such as coatings or polymers, that require specific chemical properties for enhanced durability and performance.

Analytical Chemistry: It is utilized as a standard in various analytical techniques, such as chromatography, to ensure accurate measurement and validation of other compounds in complex mixtures.

References

Novel synthetic procedures for C2 substituted imidazoquinolines as ligands for the α/β-interface of the GABAA-receptor

Publication Name: Monatshefte für Chemie - Chemical Monthly
Publication Date: 2022-10-29
DOI: 10.1007/s00706-022-02988-8

High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors

Publication Name: Antiviral Research
Publication Date: 2011-09
DOI: 10.1016/j.antiviral.2011.06.006

Synthesis, antiviral activity and molecular modeling of oxoquinoline derivatives

Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2009-08-01
DOI: 10.1016/j.bmc.2009.06.037