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Catalog Number:
40382
CAS Number:
55552-70-0
Acide 3-furylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide furan-3-boronique, Acide 3-furanylboronique
Documents
$76.51 /1G
Taille
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Informations sur le produit

3-Furylboronic acid is a versatile organoboron compound that plays a significant role in organic synthesis and medicinal chemistry. Known for its unique reactivity, this compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. Researchers and industry professionals utilize 3-Furylboronic acid to create a variety of biologically active compounds, including pharmaceuticals and agrochemicals, due to its ability to introduce the furan moiety, which is often associated with enhanced biological activity.

Additionally, 3-Furylboronic acid exhibits excellent solubility in polar solvents, making it an ideal candidate for various applications in both laboratory and industrial settings. Its stability and ease of handling further enhance its appeal for researchers looking to streamline their synthetic processes. With its potential to facilitate the development of new materials and drug candidates, 3-Furylboronic acid stands out as a crucial building block in modern chemistry.

Numéro CAS 
55552-70-0
Formule moléculaire
C4H5BO3
Poids moléculaire 
111.89
Point de fusion 
139 - 144 °C
Informations générales
Numéro CAS 
55552-70-0
Formule moléculaire
C4H5BO3
Poids moléculaire 
111.89
Point de fusion 
139 - 144 °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

3-Furylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: It serves as a key building block in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: This compound is essential in Suzuki-Miyaura coupling reactions, allowing for the formation of carbon-carbon bonds, which is crucial in creating complex molecules.
  • Fluorescent Probes: It is used in the design of fluorescent probes for biological imaging, enhancing the ability to visualize cellular processes in real-time.
  • Sensor Development: 3-Furylboronic acid is applied in the creation of sensors for detecting sugars and other biomolecules, which is valuable in food safety and medical diagnostics.
  • Material Science: Its properties make it suitable for developing advanced materials, including polymers and nanocomposites, that have applications in electronics and packaging.

Citations