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Catalog Number:
40290
CAS Number:
139911-29-8
Acide 4-fluoro-2-méthylphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-fluoro-2-méthylbenzèneboronique
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$101.45 /1G
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Informations sur le produit

4-Fluoro-2-methylphenylboronic 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, including pharmaceuticals and agrochemicals. Its unique fluorine substitution enhances its reactivity and selectivity, allowing for the development of targeted therapies and advanced materials. Researchers appreciate its role in the creation of biologically active compounds, as it can facilitate the formation of carbon-carbon bonds with high efficiency.

In addition to its applications in synthetic chemistry, 4-Fluoro-2-methylphenylboronic acid is also employed in the development of sensors and diagnostic tools due to its ability to form stable complexes with various substrates. This compound's favorable properties, such as its solubility in organic solvents and compatibility with a range of reaction conditions, make it an ideal choice for both academic and industrial applications. By incorporating this compound into your research or production processes, you can enhance the efficiency and effectiveness of your chemical transformations.

Numéro CAS 
139911-29-8
Formule moléculaire
C 7 H 8 BFO 2
Poids moléculaire 
153.95
Point de fusion 
201 °C (lit.)
Informations générales
Numéro CAS 
139911-29-8
Formule moléculaire
C 7 H 8 BFO 2
Poids moléculaire 
153.95
Point de fusion 
201 °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

4-Fluoro-2-methylphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its unique properties allow for targeted drug design, enhancing efficacy.
  • Organic Synthesis: It is commonly used in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry. This application is vital for creating complex organic molecules in materials science and drug discovery.
  • Bioconjugation: The boronic acid group can selectively bind to diols, making it useful for bioconjugation processes. This is particularly beneficial in creating targeted delivery systems in biotechnology and medical research.
  • Sensor Technology: Its ability to form complexes with sugars makes it valuable in developing biosensors for glucose monitoring, which is crucial for diabetes management and research in medical diagnostics.
  • Material Science: The compound can be incorporated into polymer matrices to enhance properties such as thermal stability and mechanical strength, making it useful in the production of advanced materials for various industrial applications.

Citations