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  2. 2,6-Dichloropyridine - Wikipedia

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

    2,6-Dichloropyridine is a chloropyridine with the formula C 5 H 3 Cl 2 N. A white solid, it is one of six isomers of dichloropyridine . It serves as a precursor to the antibiotic enoxacin , [ 2 ] as well as the drug and anpirtoline and the antifungal liranaftate .

  3. Dichloropyridine - Wikipedia

    en.wikipedia.org/wiki/Dichloropyridine

    Dichloropyridines are organic compounds with the formula Cl 2 C 5 H 3 N, consisting of a pyridine ring substituted with two chlorides. [1] Six isomers are known. They ...

  4. 2,6-Dichloroquinone-4-chloroimide - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichloroquinone-4...

    2,6-Dichloroquinone-4-chloroimide (Gibbs reagent) is an organic compound used as an colorimetric indicator to detect phenolic compounds. [1] Upon reaction with phenol itself, 2,6-dichlorophenolindophenol is formed, [ 2 ] a chemical that is used as a redox indicator .

  5. 2,6-Dichloro-4-nitroaniline - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichloro-4-nitroaniline

    2,6-Dichloro-4-nitroaniline is an organic compound with the formula O 2 NC 6 H 2 Cl 2 NH 2. It is the most widely discussed isomer of dichloronitroaniline, mainly as a precursor to the azo dye disperse brown 1. It is prepared by treatment of 4-nitroaniline with a mixture of hydrochloric acid and hydrogen peroxide (a source of chlorine). [3] [4]

  6. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    In these conversions, chloride is displaced. [2] Pyrithione, the conjugate base of 2-mercaptopyridine-N-oxide, is a fungicide found in some shampoos. Oxidation 2-chloropyridine gives 2-chloropyridine-N-oxide. [5] The antihistamine pheniramine may be generated via the reaction of phenylacetonitrile with 2-chloropyridine in the presence of a base ...

  7. Iodobenzene dichloride - Wikipedia

    en.wikipedia.org/wiki/Iodobenzene_dichloride

    Iodobenzene dichloride is hydrolyzed by basic solutions to give iodosobenzene (PhIO) [6] and is oxidized by sodium hypochlorite to give iodoxybenzene (PhIO 2). [7] In organic synthesis, iodobenzene dichloride is used as a reagent for the selective chlorination of alkenes. [1] and alkynes. [8]

  8. Diclazuril - Wikipedia

    en.wikipedia.org/wiki/Diclazuril

    This page was last edited on 8 September 2024, at 16:53 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  9. 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]