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Catalog Number:
40358
CAS Number:
762262-09-9
Acide 2-méthoxypyridine-4-boronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-méthoxy-4-pyridylboronique
Documents
$241.26 /1G
Taille
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Informations sur le produit

2-Methoxypyridine-4-boronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds, which are significant in pharmaceuticals and agrochemicals. Its unique methoxy group enhances its solubility and reactivity, allowing for more efficient coupling processes compared to other boronic acids.

Researchers and industry professionals can leverage 2-Methoxypyridine-4-boronic acid in the development of novel drug candidates and complex organic molecules. Its applications extend to the synthesis of various heterocycles and biologically active compounds, showcasing its importance in the pharmaceutical industry. Additionally, its compatibility with a range of functional groups makes it an attractive choice for chemists looking to streamline their synthetic pathways while achieving high yields.

Numéro CAS 
762262-09-9
Formule moléculaire
C6H8BNO3
Poids moléculaire 
152.94
Point de fusion 
210 - 218 °C
Informations générales
Numéro CAS 
762262-09-9
Formule moléculaire
C6H8BNO3
Poids moléculaire 
152.94
Point de fusion 
210 - 218 °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

2-Methoxypyridine-4-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases, due to its ability to form stable complexes with biologically relevant molecules.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows chemists to create complex organic molecules efficiently, making it invaluable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the preparation of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings, enhancing performance characteristics like conductivity and durability.
  • Bioconjugation: Its boronic acid functionality enables the selective labeling of biomolecules, facilitating the study of protein interactions and cellular processes, which is essential in biochemistry and molecular biology research.
  • Environmental Chemistry: It can be utilized in the development of sensors for detecting pollutants, offering a practical solution for monitoring environmental health and safety, thus contributing to sustainable practices.

Citations