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Catalog Number:
28322
CAS Number:
18706-21-3
6-Chloro-4-hydroxy-2-(trifluorométhyl)quinoléine
Purity:
≥ 97 % (HPLC)
Documents
$18.53 /1G
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Informations sur le produit

6-Chloro-4-hydroxy-2-(trifluoromethyl)quinoline is a versatile compound known for its unique trifluoromethyl group, which enhances its reactivity and solubility in various organic solvents. This compound is particularly valuable in the pharmaceutical industry, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its structural features make it an attractive candidate for developing novel therapeutic agents, especially in the fields of anti-infectives and anti-cancer drugs. Researchers have utilized this compound in studies focusing on its potential as an antimicrobial and anticancer agent, showcasing its relevance in drug discovery and development.

In addition to its pharmaceutical applications, 6-Chloro-4-hydroxy-2-(trifluoromethyl)quinoline has shown promise in agrochemical formulations, where it can be employed as a building block for creating effective crop protection agents. Its unique properties not only improve the efficacy of these formulations but also enhance their environmental compatibility. With its growing importance in both medicinal and agricultural chemistry, this compound stands out as a valuable resource for researchers and industry professionals seeking innovative solutions.

Numéro CAS 
18706-21-3
Formule moléculaire
C 10 H 5 ClF 3 NON
Poids moléculaire 
247.6
Point de fusion 
273-281 ºC
Informations générales
Numéro CAS 
18706-21-3
Formule moléculaire
C 10 H 5 ClF 3 NON
Poids moléculaire 
247.6
Point de fusion 
273-281 ºC
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

6-Chloro-4-hydroxy-2-(trifluoromethyl)quinoline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting bacterial infections and cancer. Its unique structure allows for modifications that enhance biological activity.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and fungicides. The trifluoromethyl group contributes to increased potency and selectivity, making it effective against specific pests while minimizing environmental impact.
  • Fluorescent Probes: The compound is employed in the creation of fluorescent probes for biological imaging. Its ability to absorb and emit light at specific wavelengths makes it valuable for tracking cellular processes in real-time.
  • Material Science: In the development of advanced materials, this chemical is used to enhance the properties of polymers and coatings. Its incorporation can improve thermal stability and chemical resistance, which is crucial for industrial applications.
  • Research in Biochemistry: It plays a role in biochemical research, particularly in studies related to enzyme inhibition. Understanding its interactions can lead to the development of new therapeutic agents that target specific biological pathways.

Citations