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CAS 1150271-71-8

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

Description:
2-(4-Bromo-2-fluoro-5-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 bromine and fluorine atoms on the phenyl ring contributes to its potential reactivity and influence on electronic properties, while the methoxy group can enhance solubility and stability. 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 organic synthesis. The tetramethyl substituents on the dioxaborolane ring provide steric hindrance, which may affect its reactivity and interactions with other molecules. Overall, this compound may find applications in medicinal chemistry, materials science, or as a reagent in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. Its specific characteristics, such as melting point, boiling point, and solubility, would require empirical measurement or detailed literature references for precise values.
Formula:C13H17BBrFO3
InChI:InChI=1S/C13H17BBrFO3/c1-12(2)13(3,4)19-14(18-12)8-6-11(17-5)9(15)7-10(8)16/h6-7H,1-5H3
InChI key:InChIKey=SEOPAIHMIABGAJ-UHFFFAOYSA-N
SMILES:FC=1C(B2OC(C)(C)C(C)(C)O2)=CC(OC)=C(Br)C1
Synonyms:
  • 2-(4-Bromo-2-fluoro-5-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(4-bromo-2-fluoro-5-methoxyphenyl)-4,4,5,5-tetramethyl-
  • 4-Bromo-2-fluoro-5-methoxybenzeneboronic acid, pinacol ester 96%
  • 4-Bromo-2-fluoro-5-methoxybenzeneboronic acid, pinacol ester
  • 4-Bromo-2-fluoro-5-methoxyphenylboronic acid, pinacol ester
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