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Catalog Number:
40353
CAS Number:
929250-35-1
Acide 6-benzyloxypyridine-3-boronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-benzyloxypyridine-5-boronique
Documents
$97.25 /1G
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Informations sur le produit

6-Benzyloxypyridine-3-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules. Its unique structure allows for the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals and agrochemicals. Researchers have leveraged this compound in the synthesis of biologically active molecules, showcasing its potential in drug discovery and development.

In addition to its synthetic applications, 6-Benzyloxypyridine-3-boronic acid exhibits properties that make it suitable for use in various fields, including materials science and catalysis. Its stability and reactivity under mild conditions provide researchers with a reliable tool for creating innovative compounds. As industries continue to seek efficient and effective solutions, this compound stands out for its ability to streamline synthesis processes while enhancing product yields. Whether in academic research or industrial applications, 6-Benzyloxypyridine-3-boronic acid is a valuable asset for professionals aiming to push the boundaries of chemical innovation.

Numéro CAS 
929250-35-1
Formule moléculaire
C12H12BNO3
Poids moléculaire 
229.04
Point de fusion 
110 °C (lit.)
Indice de réfraction 
n20D 1,59
Informations générales
Numéro CAS 
929250-35-1
Formule moléculaire
C12H12BNO3
Poids moléculaire 
229.04
Point de fusion 
110 °C (lit.)
Indice de réfraction 
n20D 1,59
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

6-Benzyloxypyridine-3-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies.
  • Chemical Synthesis: It is used in cross-coupling reactions, such as Suzuki-Miyaura coupling, allowing researchers to create complex organic molecules efficiently.
  • Bioconjugation: The boronic acid group enables selective binding to diols, making it useful for attaching drugs or probes to biomolecules in diagnostic applications.
  • Material Science: It plays a role in the development of new materials, including sensors and polymers, due to its ability to form stable complexes with various substrates.
  • Environmental Monitoring: The compound can be utilized in the detection of pollutants, as it can selectively bind to certain environmental contaminants, aiding in analytical chemistry.

Citations