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Catalog Number:
28284
CAS Number:
49713-47-5
Acide 4-hydroxy-6-(trifluorométhyl)quinoléine-3-carboxylique
Purity:
≥ 98 % (HPLC)
Documents
$33.45 /1G
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Product Information

4-Hydroxy-6-(trifluoromethyl)quinoline-3-carboxylic acid is a versatile compound recognized for its unique trifluoromethyl group, which enhances its chemical stability and reactivity. This compound is particularly valuable in pharmaceutical research, where it serves as a key intermediate in the synthesis of various bioactive molecules. Its ability to act as a building block for complex organic structures makes it an essential tool for medicinal chemists aiming to develop new therapeutic agents. Additionally, its hydroxyl and carboxylic acid functionalities contribute to its solubility in polar solvents, facilitating its use in diverse chemical reactions and formulations.

In the field of agrochemicals, 4-Hydroxy-6-(trifluoromethyl)quinoline-3-carboxylic acid has shown promise as a potential herbicide and fungicide, providing effective solutions for crop protection. Its unique properties allow for targeted action against specific pests while minimizing environmental impact. Researchers and industry professionals can leverage this compound's distinctive characteristics to innovate and enhance product efficacy in their formulations, making it a valuable addition to their chemical toolkit.

CAS Number
49713-47-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 11 H 6 F 3 NON 3
Molecular Weight
257.17
MDL Number
MFCD00236691
PubChem ID
2775138
Melting Point
267-274 ?C
Appearance
Poudre amorphe blanche à blanc cassé
Conditions
Conserver à 0-8°C
General Information
CAS Number
49713-47-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 11 H 6 F 3 NON 3
Molecular Weight
257.17
MDL Number
MFCD00236691
PubChem ID
2775138
Melting Point
267-274 ?C
Appearance
Poudre amorphe blanche à 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

4-Hydroxy-6-(trifluoromethyl)quinoline-3-carboxylic acid 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 therapies, due to its unique chemical structure.
  • Fluorescent Probes: Its properties make it suitable for developing fluorescent probes used in biological imaging, helping researchers visualize cellular processes in real-time.
  • Analytical Chemistry: Employed as a reagent in analytical techniques, it aids in the detection and quantification of metal ions, enhancing the accuracy of environmental monitoring.
  • Material Science: The compound is explored for its potential in creating advanced materials, including coatings and polymers, which benefit from its stability and chemical resistance.
  • Biochemical Research: It is utilized in studies of enzyme inhibition and receptor binding, providing insights into metabolic pathways and drug interactions.

Citations