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CAS 191162-40-0

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B-(1-Methyl-1H-indol-2-yl)boronic acid

Description:
B-(1-Methyl-1H-indol-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a 1-methyl-1H-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 indole structure contributes to its potential biological activity, as indole derivatives are known for their roles in pharmaceuticals and natural products. B-(1-Methyl-1H-indol-2-yl)boronic acid may also participate in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing complex organic molecules. Additionally, the compound's solubility and stability can vary depending on the solvent and pH, which are critical factors to consider in experimental applications. Overall, this compound represents a valuable tool in synthetic organic chemistry and drug development due to its unique structural features and reactivity.
Formula:C9H10BNO2
InChI:InChI=1S/C9H10BNO2/c1-11-8-5-3-2-4-7(8)6-9(11)10(12)13/h2-6,12-13H,1H3
InChI key:InChIKey=CBPBJUTWVXLSER-UHFFFAOYSA-N
SMILES:CN1C=2C(C=C1B(O)O)=CC=CC2
Synonyms:
  • (1-Methyl-1H-Ind-2-Yl)Boronic Acid
  • (1-Methyl-1H-Indol-2-Yl)Boronic Acid
  • (1-Methylindol-2-yl)boronic acid
  • 1-Methylindole-2-boronic acid
  • 2,2-Dimethyl Propane Diol-1,3-Cyclic Ester
  • Akos Brn-0885
  • B-(1-Methyl-1H-indol-2-yl)boronic acid
  • Boronic acid, (1-methyl-1H-indol-2-yl)-
  • Boronic acid, B-(1-methyl-1H-indol-2-yl)-
  • N-Methyl-2-Indoleboronic Acid
  • N-Methylindole-2-Boronic Acid
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