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CAS 1073371-98-8

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

Description:
2,5-Dichloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with two chlorine atoms and a boron-containing moiety. The presence of the dichloro groups indicates that it may exhibit significant reactivity, particularly in nucleophilic substitution reactions. The tetramethyl-1,3,2-dioxaborolane group contributes to its potential as a boron-containing reagent, which can be useful in various organic synthesis applications, including cross-coupling reactions. This compound is likely to be a solid at room temperature and may have moderate solubility in organic solvents. Its unique structure suggests potential applications in medicinal chemistry and materials science, particularly in the development of new pharmaceuticals or functional materials. Safety data should be consulted, as the chlorine substituents may pose hazards, and appropriate handling procedures should be followed. Overall, this compound represents a valuable entity in the realm of synthetic organic chemistry.
Formula:C11H14BCl2NO2
InChI:InChI=1/C11H14BCl2NO2/c1-10(2)11(3,4)17-12(16-10)8-5-7(13)6-15-9(8)14/h5-6H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cc(cnc2Cl)Cl)O1
Synonyms:
  • 2,5-Dichloropyridine-3-boronic acid pinacol ester
  • T6Nj Bg Eg C- Bt5Obotj D1 D1 E1 E1
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