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Catalog Number:
40354
CAS Number:
856250-60-7
Acide (5-fluoro-6-méthoxypyridin-3-yl)boronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-fluoro-2-méthoxypyridine-5-boronique
Documents
$127.79 /200 mg
Taille
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Informations sur le produit

(5-Fluoro-6-methoxypyridin-3-yl)boronic acid is a versatile boronic acid derivative that plays a crucial role in various fields, particularly in medicinal chemistry and organic synthesis. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique fluorine and methoxy substituents enhance its reactivity and selectivity, allowing researchers to develop targeted compounds with improved efficacy.

In addition to its synthetic applications, (5-Fluoro-6-methoxypyridin-3-yl)boronic acid has shown potential in the development of novel therapeutic agents, particularly in the treatment of cancer and other diseases. Its compatibility with various functional groups and stability under different conditions make it a preferred choice for researchers looking to innovate in drug design. With its growing importance in the pharmaceutical industry, this compound is poised to facilitate advancements in drug discovery and development.

Numéro CAS 
856250-60-7
Formule moléculaire
C6H7BFNO3
Poids moléculaire 
170.93
Informations générales
Numéro CAS 
856250-60-7
Formule moléculaire
C6H7BFNO3
Poids moléculaire 
170.93
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-Fluoro-6-methoxypyridin-3-yl)boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting cancer and infectious diseases, enhancing drug efficacy.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving specificity and reducing side effects.
  • Material Science: The compound is used in the development of advanced materials, such as sensors and catalysts, due to its unique chemical properties that facilitate efficient reactions.
  • Organic Synthesis: It acts as a versatile building block in organic synthesis, enabling the creation of complex molecules with high precision, which is essential for various chemical research applications.
  • Diagnostics: This boronic acid derivative is utilized in diagnostic assays, particularly in the detection of biomolecules, providing enhanced sensitivity and specificity in medical testing.

Citations