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  2. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    2-Chloropyridine is an aryl chloride with the formula C 5 H 4 ClN. It is a colorless liquid that is mainly used to generate fungicides and insecticides in industry. It is a colorless liquid that is mainly used to generate fungicides and insecticides in industry.

  3. Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/Chloropyridine

    Direct halogenation of pyridine with chlorine gas above 270 °C gives a mixture of 2-chloropyridine and 2,6-dichloropyridine. [1] 2- and 4-chloropyridine are prepared from the corresponding pyridinols using phosphoryl chloride. [1]

  4. 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.

  5. Category:Chloropyridines - Wikipedia

    en.wikipedia.org/wiki/Category:Chloropyridines

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  6. 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 are white or colorless, most are solids at room temperature.

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  8. Chichibabin reaction - Wikipedia

    en.wikipedia.org/wiki/Chichibabin_reaction

    The Chichibabin reaction (pronounced ' (chē')-chē-bā-bēn) is a method for producing 2-aminopyridine derivatives by the reaction of pyridine with sodium amide.It was reported by Aleksei Chichibabin in 1914. [1]

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