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Catalog Number:
24868
CAS Number:
318-35-4
6-fluoro-4-hydroxyquinoléine-3-carboxylate d'éthyle
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 6-fluoro-4-hydroxy-3-quinoléinecarboxylique
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Product Information

Ethyl 6-fluoro-4-hydroxyquinoline-3-carboxylate is a versatile compound known for its significant applications in pharmaceuticals and organic synthesis. This compound features a unique fluorine atom that enhances its biological activity, making it a valuable intermediate in the development of various therapeutic agents. Its structure allows for the potential synthesis of novel quinoline derivatives, which are of interest in medicinal chemistry due to their antimicrobial, anti-inflammatory, and anticancer properties. Researchers have utilized this compound in the synthesis of targeted drugs, showcasing its relevance in drug discovery and development.

In addition to its pharmaceutical applications, Ethyl 6-fluoro-4-hydroxyquinoline-3-carboxylate serves as a useful reagent in organic chemistry, facilitating the formation of complex molecules through various reactions. Its stability and reactivity make it an ideal candidate for researchers looking to explore new chemical pathways. With its unique properties and potential for innovation, this compound stands out as a key player in advancing both research and industrial applications.

Synonyms
Ester éthylique de l'acide 6-fluoro-4-hydroxy-3-quinoléinecarboxylique
CAS Number
318-35-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 10 FNO 3
Molecular Weight
235.21
MDL Number
MFCD00173345
PubChem ID
710779
Melting Point
> 300 °C
Appearance
Poudre blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester éthylique de l'acide 6-fluoro-4-hydroxy-3-quinoléinecarboxylique
CAS Number
318-35-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 10 FNO 3
Molecular Weight
235.21
MDL Number
MFCD00173345
PubChem ID
710779
Melting Point
> 300 °C
Appearance
Poudre blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl 6-fluoro-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 pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents.
  • Biological Research: It is used in studies investigating the mechanisms of action of quinoline derivatives, aiding researchers in understanding their biological activities and potential therapeutic effects.
  • Analytical Chemistry: The compound is employed as a standard in analytical methods, helping to calibrate instruments and validate techniques in the quantification of related compounds.
  • Material Science: Ethyl 6-fluoro-4-hydroxyquinoline-3-carboxylate finds application in the development of novel materials, particularly in coatings and polymers that require enhanced chemical stability.
  • Environmental Studies: It is utilized in research assessing the environmental impact of quinoline derivatives, contributing to the understanding of their behavior and degradation in various ecosystems.

Citations