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CAS 220465-43-0

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Indole-4-boronic acid

Description:
Indole-4-boronic acid is an organic compound characterized by the presence of both an indole ring and a boronic acid functional group. The indole structure, a bicyclic compound consisting of a benzene ring fused to a pyrrole ring, contributes to its aromatic properties and potential biological activity. The boronic acid group, featuring a boron atom bonded to a hydroxyl group and two organic groups, is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling. Indole-4-boronic acid is typically a white to off-white solid and is soluble in polar solvents. It has applications in medicinal chemistry, particularly in the development of pharmaceuticals, as well as in materials science for the synthesis of boron-containing compounds. Its reactivity and ability to participate in cross-coupling reactions make it a valuable building block in organic synthesis. Additionally, the compound's properties may be influenced by factors such as pH and the presence of other functional groups in a reaction environment.
Formula:C8H8BNO2
InChI:InChI=1/C8H8BNO2/c11-9(12)7-2-1-3-8-6(7)4-5-10-8/h1-5,10-12H
SMILES:c1cc(c2cc[nH]c2c1)B(O)O
Synonyms:
  • 1H-Indol-4-ylboronic acid
  • acide 1H-indol-4-ylboronique
  • Boronic acid, B-1H-indol-4-yl-
  • AKOS BRN-0119
  • 4-INDOLEBORONIC ACID
  • 4-INDOLYLBORONIC ACID
  • Indole-4-boronic acid ,97%
  • Indole-4-Boronic
  • 4-BORONOINDOLE
  • 1H-INDOLE-4-BORONIC ACID
  • INDOLE-4-BORONIC ACID
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