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Catalog Number:
40347
CAS Number:
871940-31-7
Acide 3-cyano-2,4-difluorophénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-cyano-2,4-difluorobenzèneboronique
Documents
$27.94 /200 mg
Taille
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Informations sur le produit

3-Cyano-2,4-difluorophenylboronic acid is a versatile compound with significant relevance in pharmaceutical and materials science applications. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block in the synthesis of complex organic molecules. Its unique structure, featuring both cyano and difluoro groups, enhances its reactivity and selectivity, which is crucial for developing targeted therapies in medicinal chemistry. Researchers have utilized this compound in the design of novel drug candidates, especially in the field of oncology, where precision and efficacy are paramount.

In addition to its pharmaceutical applications, 3-Cyano-2,4-difluorophenylboronic acid is also employed in materials science for the development of advanced polymers and sensors. Its ability to form stable complexes with various substrates allows for innovative applications in catalysis and sensor technology. The compound's distinctive properties, such as its high thermal stability and solubility in organic solvents, further enhance its utility in diverse research settings. Overall, this compound stands out for its multifunctionality and potential to drive advancements in both chemical synthesis and material development.

Numéro CAS 
871940-31-7
Formule moléculaire
C 7 H 4 BF 2 NO 2
Poids moléculaire 
182.92
Point de fusion 
134 °C (lit.)
Informations générales
Numéro CAS 
871940-31-7
Formule moléculaire
C 7 H 4 BF 2 NO 2
Poids moléculaire 
182.92
Point de fusion 
134 °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

3-Cyano-2,4-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 anti-cancer agents, due to its ability to form stable complexes with biological targets.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for constructing complex organic molecules, making it valuable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and strength, which are crucial for electronics and coatings.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, aiding in drug delivery systems and diagnostic applications.
  • Research in Chemical Biology: This compound is utilized in probing biological systems and pathways, providing insights into disease mechanisms and potential therapeutic targets, which is essential for advancing medical research.

Citations