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

  4. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    The initially formed 2-chloropyridine reacts further to give 2,6-dichloropyridine. [2] Alternatively, 2-chloropyridines can be conveniently synthesized in high yields from pyridine-N-oxides. [3] 2-Chloropyridine was originally prepared by the chlorination of 2-hydroxypyridine with phosphoryl chloride. [4]

  5. 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]

  6. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  7. 2,6-Diacetylpyridine - Wikipedia

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

    The synthesis of 2,6-diacetylpyridine begins with oxidation of the methyl groups in 2,6-lutidine to form dipicolinic acid. This process has been well established with potassium permanganate and selenium dioxide. [3] The diketone can be formed from the diester of picolinic acid groups through a Claisen condensation. [4]

  8. Dipicolinic acid - Wikipedia

    en.wikipedia.org/wiki/Dipicolinic_acid

    Dipicolinic acid (pyridine-2,6-dicarboxylic acid or PDC and DPA) is a chemical compound which plays a role in the heat resistance of bacterial endospores. It is also used to prepare dipicolinato ligated lanthanide and transition metal complexes for ion chromatography .

  9. Pyridinecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Pyridinecarboxylic_acid

    98-98-6 59-67-6 55-22-1 All isomers share the molecular weight 123,11 g/mol and the chemical formula C 6 H 5 NO 2. See also. Pyridinedicarboxylic acid