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  2. 2,3-Dichlorophenol - Wikipedia

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

    Download as PDF; Printable version; ... move to sidebar hide. 2,3-Dichlorophenol Names Preferred IUPAC name. 2,3-Dichlorophenol . Identifiers ... 2,3 -Dichlorophenol ...

  3. 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:

  4. 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

  5. 3,4-Dichlorophenol - Wikipedia

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

    Download as PDF; Printable version; In other projects ... 3,4-Dichlorophenol Names Preferred IUPAC name. 3,4-Dichlorophenol ... with the molecular formula Cl 2 C 6 H ...

  6. 2,6-Dichlorophenol - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichlorophenol

    2,6-Dichlorophenol is a compound with formula C 6 H 3 Cl 2 OH. It is one of the six isomers of dichlorophenol. It is a colorless solid. Its pK a is 6.78, which is about 100x more acidic than 2-chlorophenol (8.52) and 1000x more acidic than phenol itself (9.95). [3]

  7. 2,5-Dichlorophenol - Wikipedia

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

    Download as PDF; Printable version; In other projects ... 2,5-Dichlorophenol Names Preferred IUPAC name. 2,5-Dichlorophenol ... is a chlorinated derivative of phenol ...

  8. Dichloropyridine - Wikipedia

    en.wikipedia.org/wiki/Dichloropyridine

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Name Registry number melting point (°C) 2,3-Dichloropyridine: 2402-77-9: 203–204

  9. Dichlorophenolindophenol - Wikipedia

    en.wikipedia.org/wiki/Dichlorophenolindophenol

    The end point is a pink color that persists for 10 seconds or more, if there is not enough ascorbic acid to reduce all of the DCPIPH. Pharmacological experiments suggest that DCPIP may serve as a pro-oxidant chemotherapeutic targeting human cancer cells in an animal model of human melanoma ; DCPIP-induced cancer cell death occurs by depletion ...