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CAS 408492-27-3

:

2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Description:
2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is an organic compound characterized by its pyridine ring substituted with two chlorine atoms at the 2 and 6 positions and a boron-containing moiety at the 4 position. The presence of the dioxaborolane group contributes to its potential reactivity, particularly in cross-coupling reactions, making it valuable in synthetic organic chemistry. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, due to the electrophilic nature of the chlorinated pyridine and the boron atom's ability to form stable complexes. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, owing to its unique structural features and reactivity.
Formula:C11H14BCl2NO2
InChI:InChI=1S/C11H14BCl2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-8(13)15-9(14)6-7/h5-6H,1-4H3
InChI key:InChIKey=PEFDHAOFDBNZEQ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(Cl)N=C(Cl)C2
Synonyms:
  • (2,6-Dichloropyridin-4-yl)boronic acid pinacol ester
  • 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2,6-Dichloro-4-(pinacolboryl)pyridine
  • 2,6-Dichloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2,6-Dichloropyridine-4-boronicacidpinacolester
  • 2-(2,6-Dichloro-4-pyridinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • Pyridine, 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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