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CAS 232275-38-6

:

[4-(1,3-dioxolan-2-yl)-2,6-dimethoxyphenyl]boronic acid

Description:
[4-(1,3-Dioxolan-2-yl)-2,6-dimethoxyphenyl]boronic 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. This compound features a phenyl ring substituted with two methoxy groups and a dioxolane moiety, contributing to its unique reactivity and solubility properties. The dioxolane ring enhances the compound's stability and may influence its interaction with biological systems or other chemical entities. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. The presence of the methoxy groups can also affect the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in various chemical reactions. Overall, this compound's structure suggests potential applications in medicinal chemistry, materials science, and organic synthesis, particularly in the development of complex organic molecules.
Formula:C11H15BO6
InChI:InChI=1/C11H15BO6/c1-15-8-5-7(11-17-3-4-18-11)6-9(16-2)10(8)12(13)14/h5-6,11,13-14H,3-4H2,1-2H3
SMILES:COc1cc(cc(c1B(O)O)OC)C1OCCO1
Synonyms:
  • 4-(1,3-Dioxolan-2-yl)-2,6-dimethoxyphenylboronic acid
  • boronic acid, B-[4-(1,3-dioxolan-2-yl)-2,6-dimethoxyphenyl]-
  • [4-(1,3-Dioxolan-2-yl)-2,6-dimethoxyphenyl]boronic acid
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