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CAS 452972-11-1

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2-Chloropyridine-3-boronic acid pinacol ester

Description:
2-Chloropyridine-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a chlorinated pyridine ring. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethyl acetate. The boronic ester functionality allows for participation in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the chlorine atom on the pyridine ring can influence its reactivity and interaction with other molecules. Additionally, the pinacol ester moiety enhances the stability of the boronic acid, facilitating its handling and storage. As with many organoboron compounds, it is important to consider safety and handling precautions, as they may pose health risks if not managed properly. Overall, 2-Chloropyridine-3-boronic acid pinacol ester serves as a versatile intermediate in the synthesis of complex organic molecules.
Formula:C11H15BClNO2
InChI:InChI=1/C11H15BClNO2/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-14-9(8)13/h5-7H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccnc2Cl)O1
Synonyms:
  • Pyridine, 2-Chloro-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-
  • 2-Chloro-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
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