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CAS 1217500-61-2

:

B-(2,3-Dihydro-2-oxo-1H-indol-6-yl)boronic acid

Description:
B-(2,3-Dihydro-2-oxo-1H-indol-6-yl)boronic acid, with the CAS number 1217500-61-2, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an indole moiety. This compound typically exhibits properties associated with 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 indole structure contributes to its potential biological activity, as indole derivatives are known for their roles in pharmaceuticals. The compound is likely to be a solid at room temperature and may exhibit solubility in polar organic solvents. Its reactivity can be influenced by the presence of the boronic acid functional group, which can participate in cross-coupling reactions, making it valuable in the development of complex organic molecules. Overall, B-(2,3-Dihydro-2-oxo-1H-indol-6-yl)boronic acid represents a versatile building block in synthetic chemistry.
Formula:C8H8BNO3
InChI:InChI=1S/C8H8BNO3/c11-8-3-5-1-2-6(9(12)13)4-7(5)10-8/h1-2,4,12-13H,3H2,(H,10,11)
InChI key:InChIKey=YLNQBQVYRMHRAQ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C2C(=CC1)CC(=O)N2
Synonyms:
  • B-(2,3-Dihydro-2-oxo-1H-indol-6-yl)boronic acid
  • (2-Oxoindolin-6-yl)boronic acid
  • (2-Oxo-2,3-dihydro-1H-indol-6-yl)boronic acid
  • Boronic acid, B-(2,3-dihydro-2-oxo-1H-indol-6-yl)-
  • 2-Oxoindolin-6-ylboronic acid
  • Oxindole-6-boronic acid
  • Oxindole-6-boronic acid 95+%
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