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CAS 1253912-15-0

:

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

Description:
B-(2,3-Dihydro-1H-indol-6-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a dihydroindole 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 presence of the indole structure contributes to its potential biological activity, as indole derivatives are known for their roles in pharmaceuticals and natural products. The compound is likely to be a solid at room temperature, with solubility in polar solvents due to the boronic acid group. Its reactivity can be influenced by the pH of the environment, as boronic acids can exist in different forms depending on protonation. Overall, B-(2,3-Dihydro-1H-indol-6-yl)boronic acid is of interest for its synthetic utility and potential applications in drug development and materials science.
Formula:C8H10BNO2
InChI:InChI=1S/C8H10BNO2/c11-9(12)7-2-1-6-3-4-10-8(6)5-7/h1-2,5,10-12H,3-4H2
InChI key:InChIKey=AKTWHCRFKCLLCJ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C2C(=CC1)CCN2
Synonyms:
  • (2,3-Dihydro-1h-indol-6-yl)boronic acid
  • B-(2,3-Dihydro-1H-indol-6-yl)boronic acid
  • Boronic acid, B-(2,3-dihydro-1H-indol-6-yl)-, pinacol ester
  • Boronic acid, B-(2,3-dihydro-1H-indol-6-yl)-
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