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Catalog Number:
40306
CAS Number:
480438-58-2
Acide 2-éthoxy-4-fluorophénylboronique
Purity:
96 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-éthoxy-4-fluorobenzèneboronique
Documents
$115.27 /1G
Taille
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Informations sur le produit

2-Ethoxy-4-fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique fluorine substitution enhances its reactivity and selectivity, allowing for the development of compounds with improved biological activity. Researchers appreciate its role in creating diverse libraries of compounds for drug discovery, especially in the development of targeted therapies.

In addition to its synthetic applications, 2-Ethoxy-4-fluorophenylboronic acid has shown promise in materials science, particularly in the development of functionalized polymers and organic electronics. Its compatibility with various reaction conditions and ease of handling make it a preferred choice for both academic and industrial laboratories. With its robust performance in cross-coupling reactions and potential for innovative applications, this compound stands out as a valuable asset for professionals seeking to advance their research and development projects.

Numéro CAS 
480438-58-2
Formule moléculaire
C 8 H 10 BFO 3
Poids moléculaire 
183.97
Point de fusion 
141 °C (lit.)
Informations générales
Numéro CAS 
480438-58-2
Formule moléculaire
C 8 H 10 BFO 3
Poids moléculaire 
183.97
Point de fusion 
141 °C (lit.)
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

2-Ethoxy-4-fluorophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing pharmaceuticals, particularly in developing targeted therapies for cancer and other diseases.
  • Organic Synthesis: It is employed in various organic reactions, including Suzuki coupling, which is essential for creating complex organic molecules used in materials science and medicinal chemistry.
  • Bioconjugation: The unique properties of this boronic acid facilitate the attachment of biomolecules, aiding in the creation of bioconjugates for diagnostic and therapeutic applications.
  • Fluorescent Probes: Researchers utilize it to develop fluorescent probes that help visualize biological processes in real-time, enhancing our understanding of cellular functions.
  • Environmental Monitoring: Its ability to form stable complexes with certain environmental pollutants makes it valuable in developing sensors for detecting harmful substances in water and soil.

Citations