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Catalog Number:
40342
CAS Number:
212386-71-5
Acide 4-éthoxy-2,3-difluorophénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-éthoxy-2,3-difluorobenzèneboronique
Documents
$64.00 /1G
Taille
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Informations sur le produit

4-Ethoxy-2,3-difluorophenylboronic acid is a versatile compound known for its unique boronic acid functionality, making it an essential reagent in organic synthesis and medicinal chemistry. This compound features a difluorophenyl group, which enhances its reactivity and selectivity in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals can leverage its properties for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Its ability to form stable complexes with diols also makes it valuable in the synthesis of boron-containing compounds, which are crucial in various applications, such as drug discovery and material science.

In addition to its synthetic utility, 4-Ethoxy-2,3-difluorophenylboronic acid stands out due to its favorable solubility characteristics and compatibility with a range of solvents, which can streamline laboratory processes. This compound is particularly beneficial for those working in the field of medicinal chemistry, where it can facilitate the creation of novel therapeutic agents. Its unique structure and reactivity profile provide researchers with a powerful tool for advancing their work in organic synthesis and drug development.

Numéro CAS 
212386-71-5
Formule moléculaire
C8H9BF2O3
Poids moléculaire 
201.96
Point de fusion 
154 °C (lit.)
Informations générales
Numéro CAS 
212386-71-5
Formule moléculaire
C8H9BF2O3
Poids moléculaire 
201.96
Point de fusion 
154 °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

4-Ethoxy-2,3-difluorophenylboronic 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 targeted cancer therapies, enhancing drug efficacy and specificity.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, allowing chemists to create complex organic molecules efficiently, which is essential in materials science and agrochemicals.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation techniques for drug delivery systems and diagnostic applications, improving the precision of targeting in biological systems.
  • Material Science: This compound can be used to modify surfaces and create functional materials, such as sensors and catalysts, which are crucial in developing advanced technologies for electronics and environmental applications.
  • Research in Chemical Biology: It plays a role in studying protein interactions and cellular processes, providing insights into biochemical pathways and potential therapeutic targets, thus aiding in the advancement of biomedical research.

Citations