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Catalog Number:
40313
CAS Number:
900174-60-9
Acide 5-éthoxy-2-fluorophénylboronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 5-éthoxy-2-fluorobenzèneboronique
Documents
$79.22 /1G
Taille
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Informations sur le produit

5-Ethoxy-2-fluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals can leverage its unique properties to develop novel pharmaceuticals and agrochemicals, enhancing the efficiency of synthetic pathways. The presence of the ethoxy group contributes to its solubility and reactivity, facilitating smoother reactions and higher yields compared to similar compounds.

In addition to its synthetic applications, 5-Ethoxy-2-fluorophenylboronic acid has shown potential in the development of targeted therapies, particularly in oncology, where boron-containing compounds are being explored for boron neutron capture therapy (BNCT). Its ability to selectively bind to specific biological targets opens avenues for innovative treatment strategies. With its favorable characteristics, this compound stands out as a key player in advancing research and development in various fields, making it an indispensable tool for chemists and researchers alike.

Numéro CAS 
900174-60-9
Formule moléculaire
C 8 H 10 BFO 3
Poids moléculaire 
183.97
Point de fusion 
97 °C (lit.)
Informations générales
Numéro CAS 
900174-60-9
Formule moléculaire
C 8 H 10 BFO 3
Poids moléculaire 
183.97
Point de fusion 
97 °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

5-Ethoxy-2-fluorophenylboronic acid 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-cancer agents. Its unique boronic acid functionality allows for selective reactions that are crucial in drug formulation.
  • Organic Synthesis: It is valuable in organic chemistry for cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for constructing complex organic molecules efficiently.
  • Material Science: The compound is used in creating advanced materials, including polymers and nanomaterials, due to its ability to form stable complexes with metals, enhancing material properties.
  • Bioconjugation: In biochemistry, it is employed for labeling biomolecules, facilitating the study of protein interactions and cellular processes, which is vital for understanding disease mechanisms.
  • Diagnostics: Its application extends to the development of diagnostic agents, where it can be used to create probes for imaging techniques, aiding in the early detection of diseases.

Citations