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CAS 1309982-62-4

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2-Chloro-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Description:
2-Chloro-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is an organic compound characterized by its complex structure, which includes a pyridine ring substituted with a chlorine atom and a methyl group, as well as a boron-containing moiety. The presence of the dioxaborolane group suggests potential applications in organoboron chemistry, particularly in cross-coupling reactions, which are valuable in synthetic organic chemistry. The compound's molecular structure indicates it may exhibit unique reactivity due to the electron-withdrawing nature of the chlorine atom and the electron-donating properties of the boron-containing group. Additionally, the steric hindrance introduced by the tetramethyl substituents could influence its reactivity and solubility in various solvents. Overall, this compound may serve as a useful intermediate in the synthesis of more complex organic molecules, particularly in the development of pharmaceuticals or agrochemicals. Its specific properties, such as melting point, boiling point, and solubility, would need to be determined through experimental methods for practical applications.
Formula:C12H17BClNO2
InChI:InChI=1S/C12H17BClNO2/c1-8-6-9(10(14)15-7-8)13-16-11(2,3)12(4,5)17-13/h6-7H,1-5H3
InChI key:InChIKey=LCANKEBGLJKHTK-UHFFFAOYSA-N
SMILES:ClC1=C(B2OC(C)(C)C(C)(C)O2)C=C(C)C=N1
Synonyms:
  • 2-Chloro-5-methylpyridine-3-boronic acid pinacol ester
  • Pyridine, 2-chloro-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Chloro-5-methyl-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2-Chloro-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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