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Catalog Number:
28463
CAS Number:
63076-51-7
Acide cyclopentylboronique
Purity:
≥ 97 % (dosage par titrage)
Documents
$18.53 /1G
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Informations sur le produit

Cyclopentylboronic acid is a versatile organoboron compound known for its unique reactivity and utility in various chemical applications. This compound serves as a crucial building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with various substrates makes it an invaluable tool in Suzuki-Miyaura cross-coupling reactions, which are widely used for constructing carbon-carbon bonds. Researchers appreciate cyclopentylboronic acid for its selectivity and efficiency, allowing for the synthesis of complex molecules with minimal by-products.

In addition to its role in organic synthesis, cyclopentylboronic acid has shown promise in materials science, particularly in the development of boron-containing polymers and materials with enhanced properties. Its unique structure allows for the fine-tuning of physical and chemical properties, making it suitable for applications in sensors and electronic devices. With its growing relevance in both academic research and industrial applications, cyclopentylboronic acid stands out as a compound that can significantly enhance the efficiency and effectiveness of chemical processes.

Numéro CAS 
63076-51-7
Formule moléculaire
C 5 H 11 BO 2
Poids moléculaire 
113.95
Informations générales
Numéro CAS 
63076-51-7
Formule moléculaire
C 5 H 11 BO 2
Poids moléculaire 
113.95
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

Cyclopentylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound is a valuable reagent in the synthesis of complex organic molecules, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. Its unique structure allows for the efficient coupling of aryl halides with various nucleophiles.
  • Pharmaceutical Development: In drug discovery, cyclopentylboronic acid is used to create boron-containing compounds that can enhance the efficacy of pharmaceuticals. Its ability to form stable complexes with various biomolecules makes it a key player in medicinal chemistry.
  • Material Science: This chemical is employed in the development of advanced materials, such as polymers and nanomaterials, where boron functionality can improve mechanical properties and thermal stability.
  • Bioconjugation: In biochemistry, it serves as a tool for attaching biomolecules, such as proteins or peptides, to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Environmental Applications: Cyclopentylboronic acid can be used in environmental chemistry for the detection and removal of pollutants. Its reactivity allows for the development of sensors that can identify trace amounts of harmful substances in various environments.

Citations