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CAS 1451391-00-6

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2-[2-Fluoro-3-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-[2-Fluoro-3-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structural features, including a dioxaborolane ring and a substituted phenyl group. The presence of a fluorine atom and an ethoxy group contributes to its chemical reactivity and potential applications in organic synthesis and medicinal chemistry. This compound is likely to exhibit properties typical of boron compounds, such as Lewis acidity, which can facilitate various chemical reactions, including cross-coupling reactions in the presence of transition metals. The steric hindrance provided by the tetramethyl groups may influence its solubility and reactivity. Additionally, the compound's specific functional groups suggest potential utility in the development of pharmaceuticals or agrochemicals. As with many organoboron compounds, it may also play a role in materials science, particularly in the synthesis of polymers or as intermediates in the preparation of more complex molecules. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C15H22BFO3
InChI:InChI=1S/C15H22BFO3/c1-10(2)18-12-9-7-8-11(13(12)17)16-19-14(3,4)15(5,6)20-16/h7-10H,1-6H3
InChI key:InChIKey=DSIBMZWYVMJDAZ-UHFFFAOYSA-N
SMILES:FC1=C(B2OC(C)(C)C(C)(C)O2)C=CC=C1OC(C)C
Synonyms:
  • 2-(2-Fluoro-3-propan-2-yloxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-[2-Fluoro-3-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-[2-fluoro-3-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-
  • 2-Fluoro-3-isopropoxyphenylboronic acid pinacol ester
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