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Catalog Number:
40299
CAS Number:
313545-32-3
Acide 2-chloro-6-fluorophénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-chloro-6-fluorobenzèneboronique
Documents
$90.34 /1G
Taille
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Informations sur le produit

2-Chloro-6-fluorophenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds. Researchers and industry professionals utilize this compound in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure allows for selective functionalization, which is essential in the design of complex molecules.

In addition to its synthetic applications, 2-Chloro-6-fluorophenylboronic acid has shown promise in the field of biochemistry, particularly in the development of targeted therapies. Its ability to form stable complexes with various substrates enhances its utility in drug discovery and development. The compound's favorable reactivity profile and compatibility with a wide range of functional groups make it a preferred choice for chemists looking to streamline their synthetic pathways.

Numéro CAS 
313545-32-3
Formule moléculaire
C6H5BClFO2
Poids moléculaire 
174.36
Point de fusion 
135 °C (lit.)
Informations générales
Numéro CAS 
313545-32-3
Formule moléculaire
C6H5BClFO2
Poids moléculaire 
174.36
Point de fusion 
135 °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-Chloro-6-fluorophenylboronic 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 targeted therapies for cancer and other diseases.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows for the formation of carbon-carbon bonds, essential in creating complex organic molecules.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and strength.
  • Diagnostics: It plays a role in the design of diagnostic agents, particularly in imaging techniques that help in the early detection of diseases.
  • Research in Agrochemicals: This chemical is explored for its potential in developing new agrochemical products, improving crop protection and yield.

Citations