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  2. Pralidoxime - Wikipedia

    en.wikipedia.org/wiki/Pralidoxime

    Pralidoxime (2-pyridine aldoxime methyl chloride) or 2-PAM, usually as the chloride or iodide salts, belongs to a family of compounds called oximes that bind to organophosphate-inactivated acetylcholinesterase. [1] It is used to treat organophosphate poisoning [2] in conjunction with atropine and either diazepam or midazolam. It is a white solid.

  3. Pyridine-2-carbaldehyde - Wikipedia

    en.wikipedia.org/wiki/Pyridine-2-carbaldehyde

    Pyridine-2-carbaldehyde, also called 2-formylpyridine, is an organic compound with the formula NC 5 H 4 CHO. It is one of three isomeric pyridinaldehydes. The other isomers are pyridine-3-carboxaldehyde and pyridine-4-carboxaldehyde. Pyridine-2-carbaldehyde is a colorless oily liquid with a distinctive odor.

  4. C6H7N - Wikipedia

    en.wikipedia.org/wiki/C6H7N

    The molecular formula C 6 H 7 N (molar mass: 93.12 g/mol, exact mass: 93.0578 u) may refer to: Aniline; Azepine; Methylpyridines (picolines) 2-Methylpyridine; 3 ...

  5. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    For example, reduction with lithium aluminium hydride yields a mixture of 1,4-dihydropyridine, 1,2-dihydropyridine, and 2,5-dihydropyridine. [102] Selective synthesis of 1,4-dihydropyridine is achieved in the presence of organometallic complexes of magnesium and zinc , [ 103 ] and (Δ3,4)-tetrahydropyridine is obtained by electrochemical ...

  6. 2-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Methylpyridine

    2-Methylpyridine, or 2-picoline, is the compound described with formula C 6 H 7 N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin .

  7. Picoline - Wikipedia

    en.wikipedia.org/wiki/Picoline

    3-Methylpyridine degrades more slowly than the other two isomers, likely due to the impact of resonance in the heterocyclic ring. Like most simple pyridine derivatives, the picolines contain more nitrogen than is needed for growth of microorganisms, and excess nitrogen is generally excreted to the environment as ammonium during the degradation ...

  8. Chichibabin pyridine synthesis - Wikipedia

    en.wikipedia.org/wiki/Chichibabin_pyridine_synthesis

    The syntheses are presently conduced commercially in the presence of oxide catalysts such as modified alumina (Al 2 O 3) or silica (SiO 2). The reactants are passed over the catalyst at 350-500 °C. 2-Methylpyridine- and 4-methylpyridine are produced as a mixture from acetaldehyde and ammonia.

  9. Uvitonic acid - Wikipedia

    en.wikipedia.org/wiki/Uvitonic_acid

    Uvitonic acid (6-methyl-2,4-pyridinedicarboxylic acid) is an organic compound with the formula CH 3 C 5 H 2 N(COOH) 2. The acid is a pyridine analogue of the benzene derivative uvitic acid . [ 1 ] Under normal conditions, the acid is a white crystalline substance.