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CAS 957066-11-4

:

(6-chloro-1-methyl-indol-2-yl)boronic acid

Description:
(6-Chloro-1-methyl-indol-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to an indole derivative. This compound features a chlorine atom at the 6-position and a methyl group at the 1-position of the indole ring, contributing to its unique reactivity and properties. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the indole moiety suggests potential biological activity, as indole derivatives are often found in pharmaceuticals and natural products. Additionally, the chlorine substituent can influence the compound's electronic properties and reactivity, potentially enhancing its utility in cross-coupling reactions, such as Suzuki coupling. Overall, (6-chloro-1-methyl-indol-2-yl)boronic acid is a versatile compound with applications in synthetic chemistry and drug development, owing to its structural features and functional groups.
Formula:C9H9BClNO2
InChI:InChI=1/C9H9BClNO2/c1-12-8-5-7(11)3-2-6(8)4-9(12)10(13)14/h2-5,13-14H,1H3
SMILES:Cn1c2cc(ccc2cc1B(O)O)Cl
Synonyms:
  • (6-Chloro-1-methyl-1H-indol-2-yl)boronic acid
  • boronic acid, B-(6-chloro-1-methyl-1H-indol-2-yl)-
  • 6-Chloro-1-methylindole-2-boronicacid
  • N-methyl-6-chloroindole-2-boronic acid
  • 6-Chloro-1-methyl-1H-indole-2-boronic acid
  • 6-Chloro-1-methyl-1H-indol-2-ylboronic acid
  • 6-Chloro-1-methylindole-2-boronic acid
  • 6-chloro-1-methyl-1H-indol-2-yl-2-boronic acid
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