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  2. 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.

  3. Picoline - Wikipedia

    en.wikipedia.org/wiki/Picoline

    Picoline refers to any of three isomers of methyl pyridine (CH 3 C 5 H 4 N). They are all colorless liquids with a characteristic smell similar to that of pyridine. They are miscible with water and most organic solvents.

  4. 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]

  5. Pyridine-3-carbaldehyde - Wikipedia

    en.wikipedia.org/wiki/Pyridine-3-carbaldehyde

    Pyridine-3-carbaldehyde, also known as nicotinaldehyde, is an organic compound with the formula C 5 H 4 NCHO. It is one of three isomeric pyridinaldehydes. The other isomers are pyridine-2-carboxaldehyde and pyridine-4-carboxaldehyde. It is a colorless liquid that is routinely available commercially. It can be produced from nicotinonitrile ...

  6. 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 ...

  7. 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]

  8. Pyridine (data page) - Wikipedia

    en.wikipedia.org/wiki/Pyridine_(data_page)

    Enthalpy of combustion, Δ c H o –2782 kJ/mol Heat capacity, c p: 132.72 J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: 140 kJ/mol at 25 °C Standard molar entropy, S o gas? J/(mol K) at 25 °C Heat capacity, c p [3] 157.8 J/(mol K) at 25 °C

  9. 2-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Methylpyridine

    2-Picoline was the first pyridine compound reported to be isolated in pure form. It was isolated from coal tar in 1846 by T. Anderson. [2] This chemistry was practiced by Reilly Industries. [3] It is now mainly produced by two principal routes. One method involves the condensation of acetaldehyde and ammonia in the presence of an oxide catalyst ...