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CAS 1451391-19-7

:

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

Description:
2-(4-Bromo-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique boron-containing dioxaborolane ring structure. This compound features a phenyl group substituted with both bromine and fluorine atoms, which can influence its reactivity and interaction with other chemical species. The presence of the dioxaborolane moiety suggests potential applications in organic synthesis, particularly in cross-coupling reactions, where boron compounds are often utilized as intermediates. The bulky tetramethyl substituents contribute to the compound's steric hindrance, which may affect its solubility and reactivity. Additionally, the halogen substituents can enhance the compound's electrophilic character, making it suitable for various chemical transformations. Overall, this compound's structural features position it as a valuable building block in the development of pharmaceuticals and agrochemicals, as well as in materials science. Its specific properties, such as melting point, boiling point, and solubility, would require experimental determination for precise applications.
Formula:C12H15BBrFO2
InChI:InChI=1S/C12H15BBrFO2/c1-11(2)12(3,4)17-13(16-11)8-5-6-9(14)10(15)7-8/h5-7H,1-4H3
InChI key:InChIKey=CVLFCLUICLFWPG-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(F)=C(Br)C=C2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(4-bromo-3-fluorophenyl)-4,4,5,5-tetramethyl-
  • 2-(4-Bromo-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4-bromo-3-fluorophenylboronic acid pinacol ester
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