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Catalog Number:
28453
CAS Number:
38896-30-9
Ester méthylique de l'acide 6-quinoléinecarboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Méthylquinoléine-6-carboxylate
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Informations sur le produit

6-Quinolinecarboxylic acid methyl ester is a versatile compound widely utilized in various fields, including pharmaceuticals and agrochemicals. This methyl ester derivative of quinoline-6-carboxylic acid exhibits unique properties that make it an essential building block in the synthesis of bioactive molecules. Its structure allows for easy modification, facilitating the development of novel compounds with potential therapeutic applications. Researchers have leveraged this compound in the synthesis of anti-inflammatory agents and antimicrobial substances, showcasing its importance in drug discovery and development.

In addition to its pharmaceutical applications, 6-Quinolinecarboxylic acid methyl ester is also valuable in the agrochemical industry, where it serves as an intermediate in the production of herbicides and pesticides. Its ability to enhance the efficacy of active ingredients makes it a sought-after component in formulations aimed at improving crop yields. With its broad range of applications and the potential for further innovation, this compound stands out as a key player in advancing both health and agricultural solutions.

Numéro CAS 
38896-30-9
Formule moléculaire
C 11 H 9 NO 2
Poids moléculaire 
187.2
Informations générales
Numéro CAS 
38896-30-9
Formule moléculaire
C 11 H 9 NO 2
Poids moléculaire 
187.2
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

6-Quinolinecarboxylic acid methyl ester is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting infectious diseases and cancer. Its unique structure allows for the modification of biological activity.
  • Fluorescent Probes: It is employed in the development of fluorescent probes for biological imaging. The compound's ability to emit light under specific conditions makes it valuable in tracking cellular processes.
  • Ligand Development: In coordination chemistry, it acts as a ligand in metal complex formation. These complexes are crucial in catalysis and materials science, enhancing reaction efficiency and selectivity.
  • Research in Organic Chemistry: The compound is used in organic synthesis as a building block for creating more complex molecules, facilitating the exploration of new chemical reactions and pathways.
  • Antimicrobial Studies: Its application in antimicrobial research helps in the development of new agents against resistant strains of bacteria, addressing a significant challenge in modern medicine.

Citations