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CAS 651358-83-7

:

6-Bromopyridine-2-boronic acid pinacol ester

Description:
6-Bromopyridine-2-boronic acid pinacol ester is an organoboron compound characterized by the presence of a bromine atom and a boronic acid functional group, which is esterified with pinacol. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as dichloromethane and tetrahydrofuran. It is often utilized in organic synthesis, particularly in cross-coupling reactions, due to the reactivity of the boronic acid moiety. The presence of the bromine atom enhances its utility in various coupling reactions, including Suzuki-Miyaura coupling, which is a widely used method for forming carbon-carbon bonds. Additionally, the pinacol ester provides stability and solubility, making it easier to handle in laboratory settings. As with many organoboron compounds, it is important to handle this substance with care, as it may pose health risks if ingested or inhaled. Proper safety protocols should be followed when working with this compound in a laboratory environment.
Formula:C11H15BBrNO2
InChI:InChI=1/C11H15BBrNO2/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-9(13)14-8/h5-7H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccc(Br)n2)O1
Synonyms:
  • 2-Bromo-6-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
  • 2-Bromopyridine-6-boronic acid pinacol ester
  • 2-Bromo-6-(Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
  • 6-Bromopyridine-2-boronic acid picol ester
  • 6-BROMOPYRIDINE-2-BORONIC ACID PINACOL ESTER
  • 6-Bromo-2-pyridylboronic Acid Pinacol Ester
  • 2-(6-Bromo-2-pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 6-Bromopyridine-2-boronic acid, pinacol ester 98%
  • Pyridine, 2-bromo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 6-Bromopyridine-2-boronic...
  • See more synonyms
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