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  2. Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Dichlorophenol

    Chemical structure of 2,4-dichlorophenol. Dichlorophenols (DCPs) are any of several chemical compounds which are derivatives of phenol containing two chlorine atoms. There are six isomers: 2,3-Dichlorophenol; 2,4-Dichlorophenol; 2,5-Dichlorophenol; 2,6-Dichlorophenol; 3,4-Dichlorophenol; 3,5-Dichlorophenol

  3. 2,5-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,5-dichlorophenol

    This article about an organic halide is a stub. You can help Wikipedia by expanding it.

  4. 3,4-Dichlorophenol - Wikipedia

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

    This page was last edited on 12 December 2024, at 03:04 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. Trichlorophenol - Wikipedia

    en.wikipedia.org/wiki/Trichlorophenol

    2,4,6-Trichlorophenol, for example, has two chlorine atoms in the ortho positions and one chlorine atom in the para position. There are six different isomers: 2,3,4-Trichlorophenol

  6. C6H4Cl2O - Wikipedia

    en.wikipedia.org/wiki/C6H4Cl2O

    2,6-Dichlorophenol; 3,4-Dichlorophenol; 3,5-Dichlorophenol This page was last edited on 2 June 2020, at 16:44 (UTC). Text is available under the Creative ...

  7. Category:Phenols - Wikipedia

    en.wikipedia.org/wiki/Category:Phenols

    2,6-Dichlorophenol; 3,5-Dichlorophenol; 3,4-Dichlorophenol; Diethylamino hydroxybenzoyl hexyl benzoate; Differentiation-inducing factor; 3,5-Difluoro-4 ...

  8. Tetrachlorophenol - Wikipedia

    en.wikipedia.org/wiki/Tetrachlorophenol

    A tetrachlorophenol is any organochloride of phenol that contains four covalently bonded chlorine atoms. Tetrachlorophenols are produced by electrophilic halogenation of phenol with chlorine. [1]

  9. 2,4-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,4-Dichlorophenol

    2,4-Dichlorophenol (2,4-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH. It is a white solid that is mildly acidic (pK a = 7.9). It is produced on a large scale as a precursor to the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D).