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Catalog Number:
40297
CAS Number:
78495-63-3
Acide 2-fluoro-6-méthoxyphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-fluoro-6-méthoxybenzèneboronique
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$38.06 /1G
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Informations sur le produit

2-Fluoro-6-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals appreciate its role in the development of pharmaceuticals, agrochemicals, and advanced materials. The unique fluorine and methoxy substituents enhance its reactivity and selectivity, allowing for the efficient synthesis of complex organic molecules.

In addition to its applications in synthetic chemistry, 2-Fluoro-6-methoxyphenylboronic acid is also valuable in the field of sensor technology, where it can be employed in the detection of biomolecules. Its favorable properties, such as solubility in various organic solvents and stability under different conditions, make it an attractive choice for researchers looking to streamline their synthesis processes. With its broad range of applications and unique features, this compound stands out as a crucial tool in modern chemical research and development.

Numéro CAS 
78495-63-3
Formule moléculaire
C 7 H 8 BFO 3
Poids moléculaire 
169.95
Point de fusion 
125 °C (lit.)
Informations générales
Numéro CAS 
78495-63-3
Formule moléculaire
C 7 H 8 BFO 3
Poids moléculaire 
169.95
Point de fusion 
125 °C (lit.)
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-Fluoro-6-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases. Its unique structural features enhance the efficacy of drug candidates.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are crucial for forming carbon-carbon bonds in organic synthesis. This application is vital for creating complex molecules in the chemical industry.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.
  • Bioconjugation: In biochemistry, it facilitates the attachment of biomolecules to surfaces or other molecules, which is essential for creating biosensors and drug delivery systems.
  • Analytical Chemistry: It is utilized in the development of analytical methods for detecting and quantifying various substances, providing researchers with reliable tools for their studies.

Citations