2,3,5,6-Tetrafluorophenol
2,3,5,6-Tetrafluorophenol structure
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Common Name | 2,3,5,6-Tetrafluorophenol | ||
|---|---|---|---|---|
| CAS Number | 769-39-1 | Molecular Weight | 166.073 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 140.2±35.0 °C at 760 mmHg | |
| Molecular Formula | C6H2F4O | Melting Point | 37-39 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 79.4±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Atmospheric pressure chemical ionization of fluorinated phenols in atmospheric pressure chemical ionization mass spectrometry, tandem mass spectrometry, and ion mobility spectrometry.
J. Am. Soc. Mass Spectrom. 10(11) , 1157-65, (1999) Atmospheric pressure chemical ionization (APCI)-mass spectrometry (MS) for fluorinated phenols (C6H5-xFxOH Where x = 0-5) in nitrogen with Cl- as the reagent ion yielded product ions of M Cl- through ion associations or (M-H)- through proton abstractions. Pro... |
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Cytochrome P450-mediated oxidation of pentafluorophenol to tetrafluorobenzoquinone as the primary reaction product.
Chem. Res. Toxicol. 6(5) , 674-80, (1993) In the present study the oxidative dehalogenation of a para-halogenated phenol was studied using pentafluorophenol and its non-para-halogenated analogue 2,3,5,6-tetrafluorophenol as model compounds. 19F NMR was used to characterize the metabolite patterns. In... |
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Synthesis and radioiodination of N-Boc-p-(tri-n-butylstannyl)-L-phenylalanine tetrafluorophenyl ester: preparation of a radiolabeled phenylalanine derivative for peptide synthesis.
Bioconjug. Chem. 4(6) , 574-80, (1993) An investigation to prepare a phenylalanine derivative which could be radioiodinated and used directly in peptide synthesis was conducted. N-Boc-p-(tri-n-butylstannyl)-L-phenylalanine tetrafluorophenyl ester was targeted and synthesized from N-Boc-p-iodo-L-ph... |
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Specific and stable labeling of antibodies with technetium-99m with a diamide dithiolate chelating agent.
Proc. Natl. Acad. Sci. U. S. A. 85(11) , 4025-9, (1988) Technetium-99m labeling of antibodies has been suboptimal because of low affinity adventitious binding, nonspecific labeling, and loss of immunoreactivity. The diamide dithiolate ligand system (N2S2) forms highly stable, well-defined tetradentate complexes wi... |
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Effect of substrate and pH on the oxidative half-reaction of phenol hydroxylase.
J. Biol. Chem. 260(10) , 5998-6005, (1985) The oxidative half-reaction of phenol hydroxylase has been studied by stopped-flow spectrophotometry. Three flavin-oxygen intermediates can be detected when the substrate is thiophenol, or m-NH2, m-OH, m-CH3, m-Cl, or p-OH phenol. Intermediate I, the flavin C... |