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Catalog Number:
28906
CAS Number:
6113-62-8
Ester cyclique de l'acide 4-chlorophénylboronique
Synonym(s):
Ester cyclique de l'acide 4-chlorobenzèneboronique
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Informations sur le produit

4-Chlorophenylboronic acid, catechol cyclic ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to develop pharmaceuticals, agrochemicals, and advanced materials. Its application in the synthesis of biologically active compounds showcases its importance in drug discovery and development.

Additionally, the compound's ability to selectively bind to specific biomolecules enhances its potential in targeted drug delivery systems and diagnostic applications. With its favorable reactivity and stability, 4-Chlorophenylboronic acid, catechol cyclic ester stands out as a reliable choice for chemists seeking efficient pathways in their synthetic endeavors. Its role in facilitating the formation of carbon-carbon bonds underscores its significance in modern organic chemistry, making it a valuable asset in both research and industrial settings.

Numéro CAS 
6113-62-8
Formule moléculaire
C12H8BClO2
Poids moléculaire 
230.46
Informations générales
Numéro CAS 
6113-62-8
Formule moléculaire
C12H8BClO2
Poids moléculaire 
230.46
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-Chlorophenylboronic acid, catechol cyclic ester is widely utilized in research focused on:

  • Drug Development: This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents that target specific cellular pathways.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic compounds, making it valuable in creating complex molecules for research and industrial applications.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and drug delivery systems.
  • Sensor Technology: Its properties make it suitable for developing sensors that detect specific biomolecules, which is crucial in medical diagnostics and environmental monitoring.
  • Material Science: This chemical is utilized in the production of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings due to their unique properties.

Citations