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CAS 214360-49-3

:

1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone

Description:
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone, with the CAS number 214360-49-3, is an organic compound characterized by its unique structure that includes a phenyl group substituted with a dioxaborolane moiety. This compound typically exhibits properties associated with both aromatic and boron-containing compounds, which can influence its reactivity and stability. The presence of the dioxaborolane group suggests potential applications in organic synthesis, particularly in cross-coupling reactions, due to the boron atom's ability to participate in various chemical transformations. Additionally, the tetramethyl substituents enhance the steric bulk around the boron, potentially affecting the compound's solubility and reactivity. The ketone functional group contributes to its electrophilic character, making it a candidate for further functionalization. Overall, this compound's characteristics make it of interest in materials science and organic chemistry, particularly in the development of new synthetic methodologies and functional materials.
Formula:C14H19BO3
InChI:InChI=1/C14H19BO3/c1-10(16)11-7-6-8-12(9-11)15-17-13(2,3)14(4,5)18-15/h6-9H,1-5H3
InChI key:InChIKey=CMMASGVZWZQOEY-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(C(C)=O)=CC=C2
Synonyms:
  • 1-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethan-1-one
  • 2-(3-Acetylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • Ethanone, 1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
  • 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone
  • 2-dioxaborolan-2-yl)phenyl]ethanone
  • 1-[3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethan-1-one
  • 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone ,98%
  • 3-ACETYLPHENYLBORONIC ACID, PINACOL ESTER
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