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CAS 1220219-43-1

:

2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

Description:
2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is an organic compound characterized by the presence of a phenolic group substituted with two fluorine atoms at the 2 and 3 positions, and a boron-containing moiety at the 5 position. The compound features a dioxaborolane ring, which is known for its stability and utility in various chemical reactions, particularly in organic synthesis and as a reagent in cross-coupling reactions. The presence of fluorine atoms enhances the compound's lipophilicity and may influence its reactivity and biological activity. The tetramethyl substituents contribute to steric hindrance, potentially affecting the compound's interaction with other molecules. This compound may be of interest in medicinal chemistry and materials science due to its unique structural features and potential applications in drug development or as a building block in organic synthesis. As with many fluorinated compounds, it may exhibit distinct physical and chemical properties, such as altered solubility and reactivity compared to its non-fluorinated counterparts.
Formula:C12H15BF2O3
InChI:InChI=1S/C12H15BF2O3/c1-11(2)12(3,4)18-13(17-11)7-5-8(14)10(15)9(16)6-7/h5-6,16H,1-4H3
InChI key:InChIKey=WFXXJGVHPGKWNF-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(F)=C(F)C(O)=C2
Synonyms:
  • 2,3-Difluoro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
  • 2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
  • 3,4-Difluoro-5-hydroxyphenylboronic acid pinacol ester
  • Phenol, 2,3-difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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