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CAS 147621-18-9

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Indole-6-boronic acid

Description:
Indole-6-boronic acid is an organic compound characterized by the presence of both an indole moiety and a boronic acid functional group. The indole structure consists of a fused bicyclic system containing a benzene ring and a pyrrole ring, which contributes to its aromatic properties and biological activity. The boronic acid group, characterized by the presence of a boron atom bonded to a hydroxyl group and an alkyl or aryl group, imparts unique reactivity, particularly in forming reversible covalent bonds with diols, making it useful in various chemical applications, including drug development and materials science. Indole-6-boronic acid is often utilized in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Additionally, its derivatives have shown potential in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. The compound is typically handled with care due to its reactivity and potential environmental impact, and it is important to follow appropriate safety protocols when working with boronic acids in the laboratory.
Formula:C8H8BNO2
InChI:InChI=1/C8H8BNO2/c11-9(12)7-2-1-6-3-4-10-8(6)5-7/h1-5,10-12H
SMILES:c1cc(cc2c1cc[nH]2)B(O)O
Synonyms:
  • 6-Indoleboronic Acid
  • 6-Boronoindole
  • 1H-Indol-6-Ylboronic Acid
  • 6-Indolylboronic acid
  • 1H-Indole-6-boronic acid
  • INDOLE-6-BORONIC ACID
  • Indole-6-boronic acid 98%
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