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CAS 1165936-00-4

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2-(2-Fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(2-Fluoro-3-methoxyphenyl)-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 the fluorine atom and methoxy group on the phenyl ring contributes to its electronic properties, potentially influencing its reactivity and solubility. The dioxaborolane moiety is known for its stability and ability to participate in various chemical reactions, particularly in the context of boron chemistry, where it can act as a boron source in cross-coupling reactions. This compound may exhibit interesting properties such as moderate polarity and potential applications in organic synthesis, medicinal chemistry, or materials science. Its specific interactions and behavior in different environments would depend on factors like solvent choice and temperature. As with many boron compounds, it may also have implications in the development of new pharmaceuticals or agrochemicals, making it a subject of interest in both academic and industrial research.
Formula:C13H18BFO3
InChI:InChI=1S/C13H18BFO3/c1-12(2)13(3,4)18-14(17-12)9-7-6-8-10(16-5)11(9)15/h6-8H,1-5H3
InChI key:InChIKey=MALXDJBHSGDLGF-UHFFFAOYSA-N
SMILES:FC1=C(C=CC=C1OC)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 2-Fluoro-3-methoxyphenylboronic acid pinacol ester
  • 2-(2-Fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(2-fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-
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