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CAS 282528-62-5

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B-(5-Chloro-1H-indol-2-yl)boronic acid

Description:
B-(5-Chloro-1H-indol-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chloro-substituted indole moiety. This compound typically exhibits properties 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 chlorine atom on the indole ring can influence its reactivity and solubility, potentially enhancing its biological activity. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, this compound may exhibit interesting pharmacological properties due to the indole structure, which is often associated with various biological activities. Overall, B-(5-Chloro-1H-indol-2-yl)boronic acid is a versatile compound with potential applications in drug development and materials science.
Formula:C8H7BClNO2
InChI:InChI=1S/C8H7BClNO2/c10-6-1-2-7-5(3-6)4-8(11-7)9(12)13/h1-4,11-13H
InChI key:InChIKey=IDVLNSZYFCBHNS-UHFFFAOYSA-N
SMILES:B(O)(O)C=1NC=2C(C1)=CC(Cl)=CC2
Synonyms:
  • (5-Chloro-1H-indol-2-yl)boronic acid
  • (5-Chloro-1H-indol-2-yl)boronicacid
  • 5-Chloro-1H-Indole-2-Boronic Acid
  • B-(5-Chloro-1H-indol-2-yl)boronic acid
  • Boronic acid, (5-chloro-1H-indol-2-yl)-
  • Boronic acid, B-(5-chloro-1H-indol-2-yl)-
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