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CAS 443776-76-9

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3-(Hydroxymethyl)benzeneboronic acid pinacol ester

Description:
3-(Hydroxymethyl)benzeneboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety and a hydroxymethyl group attached to a benzene ring. This compound typically exhibits properties such as being a white to off-white solid, soluble in organic solvents like dichloromethane and ethanol, but generally insoluble in water due to its hydrophobic aromatic structure. The boronic acid functionality allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and materials science. The pinacol ester formation enhances the stability of the boronic acid, facilitating its use in reactions without the risk of hydrolysis. Additionally, this compound may exhibit moderate to low toxicity, necessitating standard safety precautions during handling. Its unique structure and reactivity profile make it a useful intermediate in the synthesis of pharmaceuticals and agrochemicals.
Formula:C13H19BO3
InChI:InChI=1/C13H19BO3/c1-12(2)13(3,4)17-14(16-12)11-7-5-6-10(8-11)9-15/h5-8,15H,9H2,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccc(c2)CO)O1
Synonyms:
  • [3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanol
  • Benzenemethanol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 3-(Hydroxymethyl)benzeneboronicacid,pinacolester96%
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl Alcohol
  • 3-Hydroxymethylphenylboronic acid, pinacol ester
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenemethanol
  • 2-(3-Hydroxymethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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