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CAS 1256359-04-2

:

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

Description:
2-Chloro-4-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its unique structure, which includes a pyridine ring substituted with both chlorine and fluorine atoms, as well as a boron-containing moiety. The presence of the tetramethyl-1,3,2-dioxaborolane group enhances its reactivity and solubility in various organic solvents, making it useful in synthetic organic chemistry, particularly in cross-coupling reactions. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions, although it should be handled with care due to the potential reactivity of the halogen substituents. Its molecular structure suggests it may participate in various chemical transformations, including nucleophilic substitutions and coordination with metal catalysts. The specific properties, such as melting point, boiling point, and solubility, would depend on the purity and specific conditions of the compound. Overall, this substance is of interest in the field of medicinal chemistry and materials science for its potential applications.
Formula:C11H14BClFNO2
InChI:InChI=1S/C11H14BClFNO2/c1-10(2)11(3,4)17-12(16-10)7-6-15-9(13)5-8(7)14/h5-6H,1-4H3
InChI key:InChIKey=DPLIDNDATZAKKG-UHFFFAOYSA-N
SMILES:FC=1C(=CN=C(Cl)C1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 2-Chloro-4-fluoro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • Pyridine, 2-chloro-4-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 6-Chloro-4-fluoropyridin-3-ylboronic acid pinacol ester
  • 2-Chloro-4-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 6-Chloro-4-fluoropyridine-3-boronic acid, pinacol ester
  • 2-Chloro-4-fluoro-5-(4,4,5,5-tetramethyl
  • 2-Chloro-4-fluoropyridine-5-boronic acid, pinacol ester
  • 2-Chloro-4-fluoro-5-(4,4,5,5-tetramethyl-195%
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