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CAS 1451391-10-8

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2-(2,6-Difluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(2,6-Difluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structure, which includes a dioxaborolane ring and a substituted phenyl group. The presence of the difluoro and nitro groups on the phenyl ring contributes to its electronic properties, potentially enhancing its reactivity and solubility in various solvents. The dioxaborolane moiety is known for its role in organic synthesis, particularly in cross-coupling reactions, making this compound of interest in medicinal chemistry and materials science. Its specific functional groups may impart unique characteristics such as increased polarity and potential for hydrogen bonding. Additionally, the compound's stability and reactivity can be influenced by the steric hindrance provided by the tetramethyl substituents. Overall, this compound exemplifies the intersection of boron chemistry and functionalized aromatic systems, offering potential applications in diverse chemical contexts.
Formula:C12H14BF2NO4
InChI:InChI=1S/C12H14BF2NO4/c1-11(2)12(3,4)20-13(19-11)9-7(14)5-6-8(10(9)15)16(17)18/h5-6H,1-4H3
InChI key:InChIKey=ROUNPYXYPTVUGB-UHFFFAOYSA-N
SMILES:FC1=C(C(F)=CC=C1N(=O)=O)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(2,6-difluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-
  • 2-(2,6-Difluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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