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CAS 648904-85-2

:

2-[3-Fluoro-4-(methylsulfonyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-[3-Fluoro-4-(methylsulfonyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structural features, including a dioxaborolane ring and a substituted phenyl group. The presence of a fluorine atom and a methylsulfonyl group on the phenyl ring contributes to its chemical reactivity and potential applications in medicinal chemistry and material science. The dioxaborolane moiety is known for its ability to participate in various chemical reactions, including Suzuki coupling, making this compound valuable in the synthesis of complex organic molecules. Additionally, the steric hindrance provided by the tetramethyl groups enhances its stability and solubility in organic solvents. This compound may exhibit interesting biological activities due to its specific functional groups, which can interact with biological targets. Overall, its unique combination of functional groups and structural characteristics makes it a subject of interest for further research in synthetic and medicinal chemistry.
Formula:C13H18BFO4S
InChI:InChI=1S/C13H18BFO4S/c1-12(2)13(3,4)19-14(18-12)9-6-7-11(10(15)8-9)20(5,16)17/h6-8H,1-5H3
InChI key:InChIKey=VRFPWIWPAXETRZ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(F)=C(S(C)(=O)=O)C=C2
Synonyms:
  • 2-[3-Fluoro-4-(methylsulfonyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-[3-Fluoro-4-(methanesulfonyl)phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
  • 3-Fluoro-4-(methylsulfonyl)phenylboronic Acid Pinacol Ester
  • 1,3,2-Dioxaborolane, 2-[3-fluoro-4-(methylsulfonyl)phenyl]-4,4,5,5-tetramethyl-
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