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  2. 2,3-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichlorophenol

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  3. Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Dichlorophenol

    3,5-Dichlorophenol Dichlorophenols are used as intermediates in the manufacture of more complex chemical compounds, including the common herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). [ 1 ]

  4. Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Trichlorophenol

    Trichlorophenols are produced by electrophilic halogenation of phenol with chlorine. [1] Different isomers of trichlorophenol exist according to which ring positions on the phenol contain chlorine atoms. 2,4,6-Trichlorophenol, for example, has two chlorine atoms in the ortho positions and one chlorine atom in the para position.

  5. 3,4-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/3,4-Dichlorophenol

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  6. 2,5-Dichlorophenol - Wikipedia

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  8. Thiophenol - Wikipedia

    en.wikipedia.org/wiki/Thiophenol

    Thiophenol is an organosulfur compound with the formula C 6 H 5 SH, sometimes abbreviated as PhSH. This foul-smelling colorless liquid is the simplest aromatic thiol.The chemical structures of thiophenol and its derivatives are analogous to phenols, where the oxygen atom in the hydroxyl group (-OH) bonded to the aromatic ring in phenol is replaced by a sulfur atom.

  9. Polyphenol - Wikipedia

    en.wikipedia.org/wiki/Polyphenol

    In the European Union, two health claims were authorized between 2012 and 2015: 1) flavanols in cocoa solids at doses exceeding 200 mg per day may contribute to maintenance of vascular elasticity and normal blood flow; [62] [63] 2) olive oil polyphenols (5 mg of hydroxytyrosol and its derivatives (e.g. oleuropein complex and tyrosol) may ...

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