Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
40266
CAS Number:
121219-16-7
Acide 2,3-difluorophénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2,3-difluorobenzèneboronique
Documents
$94.54 /5G
Taille
Request Bulk Quote
Informations sur le produit

2,3-Difluorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique fluorine substituents enhance its reactivity and selectivity, allowing for the development of complex molecular architectures. Researchers have leveraged 2,3-Difluorophenylboronic acid in the synthesis of pharmaceuticals, agrochemicals, and materials science applications, showcasing its importance in advancing chemical research and product development.

The compound's properties, including its solubility in common organic solvents and its compatibility with various functional groups, make it an attractive choice for chemists seeking efficient pathways in synthetic methodologies. Additionally, its role in the preparation of fluorinated compounds is particularly valuable in the pharmaceutical industry, where fluorine atoms can significantly influence the biological activity of drug candidates. With its proven track record in enhancing reaction outcomes, 2,3-Difluorophenylboronic acid stands out as a key player in modern synthetic chemistry.

Numéro CAS 
121219-16-7
Formule moléculaire
C6H5BF2O2
Poids moléculaire 
157.91
Point de fusion 
95 °C (déc.)
Informations générales
Numéro CAS 
121219-16-7
Formule moléculaire
C6H5BF2O2
Poids moléculaire 
157.91
Point de fusion 
95 °C (déc.)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

2,3-Difluorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases. Its unique properties enhance the efficacy of drug candidates.
  • Organic Synthesis: It is employed in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules with precision. This application is vital in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings, providing improved durability and functionality.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in drug delivery systems and diagnostic applications.
  • Research in Fluorinated Compounds: As a fluorinated boronic acid, it is valuable in studies exploring the properties and reactivity of fluorinated compounds, contributing to advancements in medicinal chemistry and materials research.

Citations