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CAS 745784-05-8

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Boronic acid, (2-bromo-3-quinolinyl)-

Description:
Boronic acid, (2-bromo-3-quinolinyl)-, identified by its CAS number 745784-05-8, is an organic compound that features a boronic acid functional group attached to a quinoline ring system. This compound typically exhibits characteristics common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and medicinal chemistry. The presence of the bromine atom in the 2-position of the quinoline ring can influence its reactivity and solubility, potentially enhancing its utility in cross-coupling reactions, such as Suzuki reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the quinoline moiety may impart biological activity, making this compound of interest in drug discovery and development. Overall, the unique structural features of (2-bromo-3-quinolinyl)boronic acid contribute to its versatility in synthetic and pharmaceutical chemistry.
Formula:C9H7BBrNO2
InChI:InChI=1S/C9H7BBrNO2/c11-9-7(10(13)14)5-6-3-1-2-4-8(6)12-9/h1-5,13-14H
InChI key:InChIKey=RUDILYIFXMOEIO-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC2=C(N=C1Br)C=CC=C2
Synonyms:
  • (2-Bromoquinolin-3-yl)boronic acid
  • Boronic acid, (2-bromo-3-quinolinyl)-
  • boronic acid, B-(2-bromo-3-quinolinyl)-
  • 2-Bromoquinoline-3-boronic acid
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