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Catalog Number:
25875
CAS Number:
31009-31-1
8-Fluoro-4-hydroxy-2-(trifluorométhyl)quinoléine
Purity:
≥ 98 % (HPLC)
Documents
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Product Information

8-Fluoro-4-hydroxy-2-(trifluoromethyl)quinoline is a versatile compound with significant applications in pharmaceutical research and development. This fluorinated quinoline derivative is recognized for its unique structural features, which enhance its biological activity and efficacy. Its trifluoromethyl group contributes to improved lipophilicity, making it an attractive candidate for drug design, particularly in the development of novel antimicrobial and antiviral agents. Researchers have explored its potential in targeting specific biological pathways, showcasing its relevance in medicinal chemistry.

In addition to its pharmaceutical applications, 8-Fluoro-4-hydroxy-2-(trifluoromethyl)quinoline serves as a valuable intermediate in the synthesis of more complex organic molecules. Its ability to undergo various chemical transformations allows for the creation of diverse derivatives, expanding its utility in materials science and agrochemicals. This compound's unique properties and versatility make it a key player in advancing research and innovation across multiple fields.

CAS Number
31009-31-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 10 H 5 F 4 NON
Molecular Weight
231.15
MDL Number
MFCD00276580
PubChem ID
2737339
Melting Point
108-117 ?C
Appearance
Poudre amorphe blanc cassé
Conditions
Conserver à 0-8°C
General Information
CAS Number
31009-31-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 10 H 5 F 4 NON
Molecular Weight
231.15
MDL Number
MFCD00276580
PubChem ID
2737339
Melting Point
108-117 ?C
Appearance
Poudre amorphe blanc cassé
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

8-Fluoro-4-hydroxy-2-(trifluoromethyl)quinoline 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-infective agents.
  • Fluorescent Probes: Its unique fluorine substitutions make it an excellent candidate for creating fluorescent probes used in biological imaging, enhancing the visibility of cellular processes.
  • Antimicrobial Research: The compound has shown promising activity against a range of pathogens, making it valuable in the search for new antimicrobial agents.
  • Material Science: It is used in the formulation of advanced materials, particularly in coatings that require enhanced chemical resistance and durability.
  • Environmental Monitoring: The compound can be applied in the detection of pollutants, aiding in environmental studies and ensuring compliance with safety regulations.

Citations