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CAS 480424-70-2

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4-Acetoxyphenylboronic acid pinacol ester

Description:
4-Acetoxyphenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group, which is typically used in organic synthesis, particularly in Suzuki coupling reactions. This compound features an acetoxy group attached to a phenyl ring, enhancing its reactivity and solubility in organic solvents. The pinacol ester moiety contributes to the stability of the boron center, making it less reactive than free boronic acids while still retaining the ability to participate in various chemical transformations. The compound is generally a white to off-white solid and is soluble in common organic solvents like dichloromethane and ethanol. Its applications extend to medicinal chemistry and materials science, where it can serve as a building block for more complex molecules. Safety data should be consulted for handling and storage, as with all organoboron compounds, due to potential reactivity and toxicity. Overall, 4-Acetoxyphenylboronic acid pinacol ester is a valuable intermediate in synthetic organic chemistry.
Formula:C14H19BO4
InChI:InChI=1S/C14H19BO4/c1-10(16)17-12-8-6-11(7-9-12)15-18-13(2,3)14(4,5)19-15/h6-9H,1-5H3
InChI key:InChIKey=KHBAJCWEQNVCSN-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(OC(C)=O)C=C2
Synonyms:
  • 4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl Acetate
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenylacetate
  • 4-(4,4,5,5-Tetramethyl-1,3-dioxaboran-2-yl)phenyl acetate
  • Phenol, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1-acetate
  • Phenol, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, acetate
  • 2-[4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate
  • 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate
  • 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL ACETATE, MIN. 97%
  • 4-ACETOXYPHENYLBORONIC ACID, PINACOL ESTER
  • 4-Acetoxybenzeneboronic acid pinacol ester
  • See more synonyms
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