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Catalog Number:
40355
CAS Number:
452972-08-6
Acide 2-bromopyridine-3-boronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 2-bromo-3-pyridylboronique
Documents
$69.60 /1G
Taille
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Informations sur le produit

2-Bromopyridine-3-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds. Researchers and industry professionals leverage its unique properties to create complex molecules, including pharmaceuticals and agrochemicals. The presence of both bromine and boronic acid functional groups enhances its reactivity, making it an ideal candidate for various coupling reactions, thus streamlining the synthesis of target compounds.

In addition to its application in synthetic chemistry, 2-Bromopyridine-3-boronic acid has shown potential in the development of novel materials and catalysts. Its ability to participate in diverse chemical transformations opens avenues for innovation in drug discovery and materials science. With its favorable characteristics, this compound stands out as a crucial building block for researchers aiming to develop new therapeutic agents or advanced materials, making it an indispensable tool in the laboratory.

Numéro CAS 
452972-08-6
Formule moléculaire
C5H5BBrNO2
Poids moléculaire 
201.81
Point de fusion 
132 °C (déc.)
Informations générales
Numéro CAS 
452972-08-6
Formule moléculaire
C5H5BBrNO2
Poids moléculaire 
201.81
Point de fusion 
132 °C (déc.)
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-Bromopyridine-3-boronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs and crop protection agents.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis, making it valuable for researchers in organic chemistry.
  • Material Science: The compound can be utilized in the development of new materials, including polymers and nanomaterials, which are important for electronics and advanced manufacturing.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation applications for drug delivery systems and targeted therapies.
  • Fluorescent Probes: Researchers leverage its properties to create fluorescent probes for biological imaging, enhancing the ability to visualize cellular processes in real-time.

Citations