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  2. Nicotinonitrile - Wikipedia

    en.wikipedia.org/wiki/Nicotinonitrile

    Nicotinonitrile or 3-cyanopyridine is an organic compound with the formula NCC 5 H 4 N. The molecule consists of a pyridine ring with a nitrile group attached to the 3-position. A colorless solid, it is produced by ammoxidation of 3-methylpyridine: [2] H 3 CC 5 H 4 N + NH 3 + 1.5 O 2 → NCC 5 H 4 N + 3 H 2 O. Nicotinonitrile is a precursor to ...

  3. Mirtazapine - Wikipedia

    en.wikipedia.org/wiki/Mirtazapine

    The first step of synthesis is a condensation reaction between the molecule 2-chloro 3-cyanopyridine and the molecule 1-methyl-3-phenylpiperazine. [121] History

  4. 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 ...

  5. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-Picoline is a useful precursor to agrochemicals, such as chlorpyrifos. [1] Chlorpyrifos is produced from 3,5,6-trichloro-2-pyridinol, which is generated from 3-picoline by way of cyanopyridine. This conversion involves the ammoxidation of 3-methylpyridine: CH 3 C 5 H 4 N + 1.5 O 2 + NH 3 → NCC 5 H 4 N + 3 H 2 O

  6. Pyridinecarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Pyridinecarboxylic_acid

    2-pyridinecarboxylic acid 3-pyridinecarboxylic acid 4-pyridinecarboxylic acid Structural Formula: CAS Registry Number: 98-98-6 59-67-6 55-22-1

  7. 3-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/3-Chloropyridine

    3-Chloropyridine is an aryl chloride and isomer of chloropyridine with the formula C 5 H 4 ClN. It is a colorless liquid that is mainly used as a building block in organic synthesis. [1] The compound is a substrate for many coupling processes including the Heck reaction, [2] Suzuki reaction, [3] and Ullmann reaction. [4]

  8. Can alcohol cause cancer? Here's what the science says

    www.aol.com/alcohol-cause-cancer-heres-science...

    A growing body of evidence has shown links between cancer and drinking alcohol. In a warning Friday, U.S. Surgeon General Vivek Murthy said cancer risk increases with the number of drinks, but ...

  9. Pyridine-N-oxide - Wikipedia

    en.wikipedia.org/wiki/Pyridine-N-oxide

    Protonated derivatives are isolable, e.g., [C 5 H 5 NOH]Cl. [3] Further demonstrating its (feeble) basicity, pyridine-N-oxide also serves as a ligand in coordination chemistry. A host of transition metal complexes of pyridine-N-oxides are known. Treatment of the pyridine-N-oxide with phosphorus oxychloride gives 4- and 2-chloropyridines. [8]