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Description
General description
Tetrafluoro-1,4-benzoquinone causes coupling of two alcohols via the oxidation-reduction condensation for the preparation of symmetrical or unsymmetrical ethers. Tetrafluoro-1,4-benzoquinone forms chiral and racemic charge transfer complex with 1,1′-bi-2-naphthol system. Tetrafluoro-1,4-benzoquinone generates 2,3,5,6-tetramethoxy-1,4-benzosemiquinone transient radical which can be detected by EPR spectroscopy.
Application
Tetrafluoro-1,4-benzoquinone was used in a study to evaluate molecular mechanism for transition metal ion independent production of hydroxyl radicals from H2O2 and halogenated quinones.
Packaging
1, 5 g in glass bottle
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