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Catalog Number:
40374
CAS Number:
850991-69-4
Acide 5-méthoxypyridine-3-boronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 5-méthoxy-3-pyridylboronique
Documents
$129.19 /1G
Taille
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Informations sur le produit

5-Methoxypyridine-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 development of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique methoxy group enhances solubility and reactivity, allowing for efficient coupling with various electrophiles. Researchers appreciate its role in synthesizing biologically active compounds, where it can contribute to the creation of novel drug candidates with improved efficacy.

In addition to its synthetic applications, 5-Methoxypyridine-3-boronic acid is also explored for its potential in material science, particularly in the development of functionalized polymers and sensors. Its favorable properties, such as stability and compatibility with various reaction conditions, make it a preferred choice for chemists looking to innovate in their respective fields. Whether you are involved in drug discovery or materials research, this compound offers significant advantages in efficiency and versatility.

Numéro CAS 
850991-69-4
Formule moléculaire
C6H8BNO3
Poids moléculaire 
152.94
Point de fusion 
230 - 270 °C
Informations générales
Numéro CAS 
850991-69-4
Formule moléculaire
C6H8BNO3
Poids moléculaire 
152.94
Point de fusion 
230 - 270 °C
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

5-Methoxypyridine-3-boronic acid 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.
  • Medicinal Chemistry: It is used in the design of new drug candidates, especially for targeting specific biological pathways, enhancing the efficacy of treatments in areas like cancer and infectious diseases.
  • Material Science: The compound plays a crucial role in the development of advanced materials, including polymers and nanomaterials, due to its unique boronic acid functionality.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Cross-Coupling Reactions: This chemical is integral in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds in organic chemistry.

Citations