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CAS 1073353-78-2

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2,3-Dichloropyridine-4-boronic acid pinacol ester

Description:
2,3-Dichloropyridine-4-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyridine ring substituted with two chlorine atoms at the 2 and 3 positions and a boronic acid moiety that is esterified with pinacol. This compound typically exhibits properties associated with both boronic acids and chlorinated heterocycles, such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, particularly in Suzuki-Miyaura coupling. The boronic ester functionality allows for the formation of stable complexes with diols and can participate in various organic transformations. Additionally, the presence of chlorine substituents can influence the electronic properties of the molecule, affecting its reactivity and interaction with other chemical species. This compound is of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its potential utility in forming carbon-carbon bonds and as a building block for more complex molecules.
Formula:C11H14BCl2NO2
InChI:InChI=1/C11H14BCl2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-6-15-9(14)8(7)13/h5-6H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccnc(c2Cl)Cl)O1
Synonyms:
  • 2,3-Dichloro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
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