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Catalog Number:
40391
CAS Number:
2096333-73-0
Chlorhydrate d'acide 2-méthylpyridine-5-boronique
Purity:
≥ 98%
Synonym(s):
Chlorhydrate d'acide 6-méthyl-3-pyridylboronique
Documents
$181.67 /1G
Taille
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Informations sur le produit

2-Methylpyridine-5-boronic acid hydrochloride 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 forming carbon-carbon bonds in the development of pharmaceuticals and agrochemicals. Its unique structure allows for the selective functionalization of aromatic compounds, making it an indispensable tool for researchers aiming to create complex molecules with precision.

In addition to its synthetic applications, 2-Methylpyridine-5-boronic acid hydrochloride exhibits potential in the development of targeted therapies, particularly in the field of cancer research. Its ability to form stable complexes with various substrates enhances its utility in drug discovery and development. Researchers and industry professionals will find this compound beneficial for its efficiency in facilitating reactions that lead to the synthesis of novel compounds, thus accelerating the pace of innovation in chemical research and development.

Numéro CAS 
2096333-73-0
Formule moléculaire
C6H8BNO2 · HCl
Poids moléculaire 
173.4
Informations générales
Numéro CAS 
2096333-73-0
Formule moléculaire
C6H8BNO2 · HCl
Poids moléculaire 
173.4
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-Methylpyridine-5-boronic acid hydrochloride is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, allowing for the formation of carbon-carbon bonds, which is essential in creating complex organic structures.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation processes for drug delivery systems and targeted therapies.
  • Material Science: This compound is applied in the development of advanced materials, including sensors and catalysts, due to its unique chemical properties that enhance performance.
  • Analytical Chemistry: It is utilized in various analytical techniques, such as chromatography, to improve the separation and detection of biomolecules, aiding in research and quality control.

Citations