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CAS 380151-85-9

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2-Formylbenzeneboronic acid pinacol ester

Description:
2-Formylbenzeneboronic acid pinacol ester, with the CAS number 380151-85-9, is an organoboron compound characterized by the presence of both a boronic acid moiety and an aldehyde functional group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as dichloromethane and ethanol. Its structure features a phenyl ring substituted with a formyl group and a boronic acid pinacol ester, which enhances its reactivity in various chemical transformations. 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. Additionally, the presence of the aldehyde group can facilitate further functionalization, enabling the synthesis of more complex molecules. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and the creation of novel materials. Proper handling and storage are essential, as with many organoboron compounds, to ensure stability and reactivity.
Formula:C13H17BO3
InChI:InChI=1/C13H17BO3/c1-12(2)13(3,4)17-14(16-12)11-8-6-5-7-10(11)9-15/h5-9H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccccc2C=O)O1
Synonyms:
  • 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
  • Benzaldehyde, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Formylphenylboronic acid pinacol ester
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