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Catalog Number:
27707
CAS Number:
63010-69-5
Ethyl 8-fluoro-4-hydroxy-3-quinolinecarboxylate
Synonym(s):
8-Fluoro-4-hydroxyquinoline-3-carboxylic acid ethyl ester
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Product Information

Ethyl 8-fluoro-4-hydroxy-3-quinolinecarboxylate is a versatile compound known for its significant applications in pharmaceutical research and development. This compound features a unique fluorine substitution that enhances its biological activity, making it a valuable candidate in the synthesis of novel therapeutic agents. Researchers have explored its potential in developing anti-inflammatory and antimicrobial drugs, leveraging its ability to interact with biological targets effectively.

In addition to its medicinal applications, Ethyl 8-fluoro-4-hydroxy-3-quinolinecarboxylate is also utilized in the field of organic synthesis, where it serves as an intermediate in the preparation of complex molecules. Its favorable solubility and stability under various conditions make it an attractive choice for chemists looking to streamline their synthetic pathways. With its unique properties and broad applicability, this compound stands out as a key ingredient in advancing both research and industrial processes.

Synonyms
8-Fluoro-4-hydroxyquinoline-3-carboxylic acid ethyl ester
CAS Number
63010-69-5
Molecular Formula
C12H10FNO3
Molecular Weight
235.21
MDL Number
MFCD00173363
PubChem ID
707160
Conditions
Store at 0-8°C
General Information
Synonyms
8-Fluoro-4-hydroxyquinoline-3-carboxylic acid ethyl ester
CAS Number
63010-69-5
Molecular Formula
C12H10FNO3
Molecular Weight
235.21
MDL Number
MFCD00173363
PubChem ID
707160
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 8-fluoro-4-hydroxy-3-quinolinecarboxylate 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 and cancer, enhancing drug efficacy.
  • Antimicrobial Research: Its unique structure contributes to its effectiveness against a range of pathogens, making it valuable in the development of new antimicrobial agents.
  • Fluorescent Probes: The compound's fluorescent properties allow it to be used in biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Material Science: It can be incorporated into polymers to create materials with enhanced properties, such as improved thermal stability and UV resistance, beneficial for various industrial applications.
  • Biochemical Assays: This chemical is utilized in assays to study enzyme activity and interactions, providing insights that are crucial for drug discovery and development.

Citations