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CAS 642494-37-9

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Indole-7-boronic acid pinacol ester

Description:
Indole-7-boronic acid pinacol ester is an organoboron compound characterized by the presence of both an indole moiety and a boronic acid functional group, which is protected by a pinacol ester. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and methanol. The boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The indole structure contributes to its potential biological activity, as indoles are known for their presence in various natural products and pharmaceuticals. Additionally, the pinacol ester serves as a protective group, enhancing the stability of the boronic acid under certain conditions. Overall, Indole-7-boronic acid pinacol ester is a versatile compound in synthetic organic chemistry, with applications in drug discovery and material science.
Formula:C14H18BNO2
InChI:InChI=1/C14H18BNO2/c1-13(2)14(3,4)18-15(17-13)11-7-5-6-10-8-9-16-12(10)11/h5-9,16H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccc3cc[nH]c23)O1
Synonyms:
  • 7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
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