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CAS 867044-33-5

:

[4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid

Description:
[4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid, with the CAS number 867044-33-5, is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl group and a benzimidazole moiety, contributing to its potential applications in medicinal chemistry and materials science. The boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the benzimidazole structure may impart biological activity, as benzimidazoles are often associated with various pharmacological properties. The compound is typically a solid at room temperature and may exhibit solubility in polar organic solvents. Its reactivity and functional versatility make it a subject of interest in research focused on drug development and organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C19H15BN2O2
Synonyms:
  • 4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenylboronic acid
  • [4-(2-Phenyl-1H-benzimidazol-1-yl)phenyl]boronic acid
  • [4-(2-phenyl-1H-1,3-benzodiazol-1-yl)phenyl]boronic acid
  • 3-(2-phenyl-1H-benzo[d]imidazol-1-yl)phenyl
  • Boronicacid, [4-(2-phenyl-1H-benziMidazol-1-yl)phenyl]- (9CI)
  • [4-(2-Phenyl-1H-benziMidazol-1-yl)phenyl]boronic acid
  • 4-(2-Phenyl-1H-benzimidazol-1-yl)benzeneboronic Acid
  • (PBIPBA
  • (4-(2-Phenyl-1H-benzo[d]imidazol-1-yl)
  • 4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid (contains varying amounts of Anhydride)
  • See more synonyms
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