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CAS 1073371-78-4

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Pyridine, 2,6-dichloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

Description:
Pyridine, 2,6-dichloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of dichloro substituents at the 2 and 6 positions of the pyridine ring indicates that it has enhanced reactivity and potential applications in various chemical reactions, particularly in synthesis. The 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl group introduces a boron-containing moiety, which can facilitate reactions such as Suzuki coupling, making this compound valuable in organic synthesis and materials science. The compound's structure suggests it may exhibit unique electronic properties due to the combination of the electron-withdrawing chlorine atoms and the electron-rich boron moiety. Additionally, the presence of multiple functional groups may influence its solubility, stability, and reactivity in different solvents and under various conditions. Overall, this compound is of interest for its potential applications in pharmaceuticals, agrochemicals, and advanced materials.
Formula:C11H14BCl2NO2
InChI:InChI=1S/C11H14BCl2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-6-8(13)15-9(7)14/h5-6H,1-4H3
InChI key:InChIKey=AOLXLWZJOQBPQX-UHFFFAOYSA-N
SMILES:ClC1=C(C=CC(Cl)=N1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 2,6-Dichloro-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2,6-Dichloropyridine-3-boronicacidpinacolester
  • 2,6-Dichloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • Pyridine, 2,6-dichloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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