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Catalog Number:
40386
CAS Number:
62306-79-0
Acide 5-méthyl-2-furanboronique
Purity:
96 - 105 % (dosage par titrage)
Synonym(s):
Acide 5-méthyl-2-furylboronique
Documents
$88.93 /1G
Taille
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Informations sur le produit

5-Methyl-2-furanboronic acid is a versatile boronic acid derivative that plays a significant role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds. Its unique furan ring structure enhances its reactivity and compatibility with various substrates, allowing for the development of complex molecules in pharmaceutical research. Additionally, 5-Methyl-2-furanboronic acid serves as a key intermediate in the synthesis of biologically active compounds, including potential drug candidates, thereby supporting advancements in therapeutic applications.

Researchers and industry professionals can leverage the properties of 5-Methyl-2-furanboronic acid for the development of novel materials and pharmaceuticals. Its ease of use in synthetic pathways and the ability to fine-tune molecular properties make it an attractive choice for those looking to innovate in chemical synthesis. With its growing relevance in the field, this compound stands out as a crucial tool for enhancing research outcomes and driving forward the development of new chemical entities.

Numéro CAS 
62306-79-0
Formule moléculaire
C 5 H 7 BO 3
Poids moléculaire 
125.92
Point de fusion 
82 °C (lit.)
Informations générales
Numéro CAS 
62306-79-0
Formule moléculaire
C 5 H 7 BO 3
Poids moléculaire 
125.92
Point de fusion 
82 °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

5-Methyl-2-furanboronic 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.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex carbon-carbon bonds efficiently, which is essential in drug discovery.
  • Sensor Development: The unique properties of this boronic acid make it suitable for developing chemical sensors, particularly for detecting sugars and other biomolecules, enhancing biosensing technologies.
  • Material Science: It is utilized in the formulation of advanced materials, including polymers and coatings, due to its ability to modify the physical properties of materials, leading to improved performance.
  • Medicinal Chemistry: Researchers leverage its reactivity to design and optimize drug candidates, particularly in targeting specific biological pathways, which can lead to more effective treatments.

Citations