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CAS 452972-12-2

:

2-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Description:
2-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with a bromine atom and a boron-containing dioxaborolane moiety. The presence of the bromine atom introduces electrophilic properties, making it useful in various synthetic applications, particularly in cross-coupling reactions. The dioxaborolane group enhances the compound's reactivity and stability, facilitating its use in organic synthesis, especially in the formation of carbon-boron bonds. This compound is typically utilized in medicinal chemistry and materials science due to its potential in creating complex molecular architectures. Its solubility and stability in various solvents can vary, influencing its application in different chemical environments. Additionally, the presence of the tetramethyl substituents contributes to steric hindrance, which can affect the reactivity and selectivity in chemical reactions. Overall, 2-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C11H15BBrNO2
InChI:InChI=1S/C11H15BBrNO2/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-14-9(8)13/h5-7H,1-4H3
InChI key:InChIKey=QAQDSIBZRCSYAR-UHFFFAOYSA-N
SMILES:BrC1=C(B2OC(C)(C)C(C)(C)O2)C=CC=N1
Synonyms:
  • 2-(2-Bromo-3-pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-Bromo-3-Pyridineboronic Acid Pinacol Ester
  • Pyridine, 2-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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