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CAS 214360-62-0

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2-Bromo-5-pyridylboronic acid pinacol ester

Description:
2-Bromo-5-pyridylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety and a pyridine ring. This compound typically features a bromine atom at the 2-position of the pyridine ring, which can enhance its reactivity in various chemical transformations, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The pinacol ester functionality provides stability to the boronic acid group, making it more suitable for storage and handling. This compound is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to form carbon-carbon bonds. Additionally, the presence of the pyridine ring can impart unique electronic properties, influencing the reactivity and selectivity in chemical reactions. Overall, 2-Bromo-5-pyridylboronic acid pinacol ester is a valuable intermediate in synthetic organic chemistry, facilitating the construction of complex molecular architectures.
Formula:C11H15BBrNO2
InChI:InChI=1/C11H15BBrNO2/c1-10(2)11(3,4)16-12(15-10)8-5-6-9(13)14-7-8/h5-7H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(Br)nc2)O1
Synonyms:
  • 2-Brom-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin
  • 2-Bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • Pyridine, 2-Bromo-5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-
  • 2-Bromopyridine-5-boronicacidpinacolester
  • 2-Bromopyridine-5-boronic acid pinacol ester
  • 6-Bromopyridine-3-boronic acid pinacol ester
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