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  2. 4-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/4-Methylpyridine

    4-Methylpyridine is the organic compound with the formula CH 3 C 5 H 4 N. It is one of the three isomers of methylpyridine. This pungent liquid is a building block for the synthesis of other heterocyclic compounds. Its conjugate acid, the 4-methylpyridinium ion, has a pK a of 5.98, about 0.7 units above that of pyridine itself. [1]

  3. Methylpyridinium - Wikipedia

    en.wikipedia.org/wiki/Methylpyridinium

    Methylpyridinium is prepared by treating pyridine with dimethylsulfate: [2]. C 5 H 5 N + (CH 3 O) 2 SO 2 → [C 5 H 5 NCH 3] + CH 3 OSO − 3. It is found in some coffee products. [3] It is not present in unroasted coffee beans, but is formed during roasting from its precursor chemical, trigonelline. [3]

  4. 2,6-Di-tert-butylpyridine - Wikipedia

    en.wikipedia.org/wiki/2,6-Di-tert-butylpyridine

    Print/export Download as PDF; ... Names Preferred IUPAC name. ... and 2,6-di-tert-butyl-4-methylpyridine. [4] See also

  5. Isonicotinic acid - Wikipedia

    en.wikipedia.org/wiki/Isonicotinic_acid

    Isonicotinic acid or pyridine-4-carboxylic acid is an organic compound with the formula C 5 H 4 N(CO 2 H). It is a derivative of pyridine with a carboxylic acid substituent at the 4-position. It is an isomer of picolinic acid and nicotinic acid , which have the carboxyl group at the 2- and 3-position respectively compared to the 4-position for ...

  6. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-Methylpyridine or 3-picoline, is an organic compound with formula 3-CH 3 C 5 H 4 N. It is one of three positional isomers of methylpyridine, whose structures vary according to where the methyl group is attached around the pyridine ring. This colorless liquid is a precursor to pyridine derivatives that have applications in the pharmaceutical ...

  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. Category:Pyridines - Wikipedia

    en.wikipedia.org/wiki/Category:Pyridines

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  9. 5-pyridoxate dioxygenase - Wikipedia

    en.wikipedia.org/wiki/5-pyridoxate_dioxygenase

    The oxygen incorporated need not be derived from O2 with NADH or NADPH as one donor, and incorporation of two atoms o oxygen into the other donor. The systematic name of this enzyme class is 5-pyridoxate,NADPH:oxygen oxidoreductase (decyclizing). This enzyme is also called 5-pyridoxate oxidase. This enzyme participates in vitamin B 6 metabolism.