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CAS 162356-89-0

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[4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid

Description:
[4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic acid] is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a silyl ether group, which enhances its stability and solubility in organic solvents. The presence of the tert-butyl group contributes to steric hindrance, influencing its reactivity and interactions with other molecules. This compound is typically utilized in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, and may also serve as a building block in the synthesis of more complex organic structures. Its unique structural features allow for specific interactions in biological systems, making it a candidate for drug development and material science applications. As with many organoboron compounds, careful handling and storage are recommended due to potential reactivity and sensitivity to moisture.
Formula:C13H23BO3Si
InChI:InChI=1/C13H23BO3Si/c1-13(2,3)18(4,5)11-6-7-12(14(16)17)10(8-11)9-15/h6-8,15-17H,9H2,1-5H3
SMILES:CC(C)(C)[Si](C)(C)c1ccc(c(c1)CO)B(O)O
Synonyms:
  • 4-TBSMS-hydroxymethylphenylboronic acid
  • [4-[[[tert-Butyl)dimethylsilyl]oxy]methyl]phenylboronic acid
  • Boronic acid, B-[4-[[[(1,1-diMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-
  • 4-TBDMSO-methylphenylboronic acid
  • [4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid
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