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CAS 458532-90-6

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3-Chloropyridine-4-boronic acid pinacol ester

Description:
3-Chloropyridine-4-boronic acid pinacol ester is an organoboron compound characterized by the presence of a chlorinated pyridine ring and a boronic acid moiety esterified with pinacol. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethanol. It is often utilized in organic synthesis, particularly in cross-coupling reactions, due to the reactivity of the boronic acid functional group, which can form carbon-carbon bonds with various electrophiles. The chloropyridine structure contributes to its unique electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, the pinacol ester form enhances stability and solubility, facilitating its handling and application in laboratory settings. As with many organoboron compounds, it is important to handle this substance with care, adhering to safety protocols to mitigate any potential hazards associated with its use.
Formula:C11H15BClNO2
InChI:InChI=1/C11H15BClNO2/c1-10(2)11(3,4)16-12(15-10)8-5-6-14-7-9(8)13/h5-7H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccncc2Cl)O1
Synonyms:
  • 3-Chloro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
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