CymitQuimica logo

CAS 1218791-09-3

:

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

Description:
2-(4-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon atom, forming a cyclic arrangement. The presence of the 4-fluoro-3-nitrophenyl group introduces significant electronic and steric effects, influencing the compound's reactivity and potential applications in organic synthesis and medicinal chemistry. This compound is likely to exhibit properties typical of boron-containing compounds, such as Lewis acidity, which can facilitate various chemical reactions, including cross-coupling reactions. Additionally, the nitro and fluoro substituents can enhance its solubility and stability in different solvents, making it suitable for diverse chemical environments. Its unique structure may also confer specific biological activities, making it of interest in pharmaceutical research. Overall, this compound represents a valuable building block in the synthesis of more complex organic molecules.
Formula:C12H15BFNO4
InChI:InChI=1S/C12H15BFNO4/c1-11(2)12(3,4)19-13(18-11)8-5-6-9(14)10(7-8)15(16)17/h5-7H,1-4H3
InChI key:InChIKey=QBMHYMHOXGOPAF-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(N(=O)=O)=C(F)C=C2
Synonyms:
  • 2-(4-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(4-fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-
  • 3-Hydroxy-2,3-dimethylbutan-2-yl hydrogen (4-fluoro-3-nitrophenyl)boronate
  • 2-(4-Fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene
  • 4-Fluoro-3-nitrophenylboronic acid, pinacol ester
  • 4-Fluoro-3-nitrobenzeneboronic acid, pinacol ester 95%
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.