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Catalog Number:
40378
CAS Number:
867044-33-5
Acide 4-(2-phényl-1 H -benzimidazol-1-yl)phénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-(2-phényl-1 H -benzimidazol-1-yl)benzèneboronique
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$263.29 /1G
Taille
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Informations sur le produit

4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic acid is a versatile compound known for its unique properties that make it invaluable in various research and industrial applications. This boronic acid derivative is recognized for its ability to form stable complexes with diols, which is particularly beneficial in the development of sensors and catalysts. Its structural features allow it to act as a key building block in organic synthesis, enabling the creation of complex molecular architectures. Researchers have utilized this compound in medicinal chemistry, particularly in the design of targeted therapies and drug delivery systems, owing to its potential to enhance bioavailability and efficacy of pharmaceutical agents.

In addition to its applications in drug development, 4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic acid is also employed in materials science, where it contributes to the development of advanced materials with tailored properties. Its ability to participate in cross-coupling reactions makes it a valuable reagent in the synthesis of functionalized organic compounds. With its diverse applications and significant advantages over similar compounds, this boronic acid is an essential tool for researchers and industry professionals seeking innovative solutions in their projects.

Numéro CAS 
867044-33-5
Formule moléculaire
C19H15BN2O2
Poids moléculaire 
314.15
Informations générales
Numéro CAS 
867044-33-5
Formule moléculaire
C19H15BN2O2
Poids moléculaire 
314.15
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-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic acid is widely utilized in research focused on:

  • Medicinal Chemistry: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in developing targeted cancer therapies due to its ability to interact with specific biological targets.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows for the formation of carbon-carbon bonds, essential for creating complex organic molecules.
  • Bioconjugation: The boronic acid functionality enables the selective labeling of biomolecules, facilitating the study of protein interactions and dynamics in biological research.
  • Sensor Development: This compound can be used in the fabrication of sensors for detecting glucose and other biomolecules, providing a vital tool for diabetes management and other health monitoring applications.
  • Material Science: It is also explored in the development of advanced materials, such as polymers and nanomaterials, which can have applications in electronics and photonics.

Citations