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  2. 3-Hydroxyisonicotinaldehyde - Wikipedia

    en.wikipedia.org/wiki/3-Hydroxyisonicotinaldehyde

    3-Hydroxyisonicotinaldehyde (HINA), also known as 3-hydroxypyridine-4-carboxaldehyde, is a derivative of pyridine, with hydroxyl and aldehyde substituents. It has been studied as a simple analogue of vitamin B 6. In 2020, it was reported as having the lowest molecular weight of all dyes which exhibit green fluorescence. [2] [3]

  3. 2-Pyridone - Wikipedia

    en.wikipedia.org/wiki/2-Pyridone

    The amide group can be involved in hydrogen bonding to other nitrogen- and oxygen-containing species.. The predominant solid state form is 2-pyridone. This has been confirmed by X-ray crystallography which shows that the hydrogen in solid state is closer to the nitrogen than to the oxygen (because of the low electron density at the hydrogen the exact positioning is difficult), and IR ...

  4. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Pyridine and poly(4-vinyl) pyridine have been shown to form conducting molecular wires with remarkable polyenimine structure on UV irradiation, a process which accounts for at least some of the visible light absorption by aged pyridine samples. These wires have been theoretically predicted to be both highly efficient electron donors and ...

  5. 4-Pyridone - Wikipedia

    en.wikipedia.org/wiki/4-Pyridone

    4-Pyridone exists a keto-enol tautomerism with its enol tautomer 4-hydroxypyridine. In solution, the keto tautomer is favoured, [4] and the enol tautomer only becomes important in very dilute solutions or solutions of non-polar solvents. However, the enol tautomer is dominant in the gas phase. [5]

  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. MoOPH - Wikipedia

    en.wikipedia.org/wiki/MoOPH

    It is an electrophilic source of oxygen that reacts with enolates and related structures, and thus can be used for alpha-hydroxylation of carbonyl-containing compounds. [3] Other reagents used for alpha-hydroxylation via enol or enolate structures include Davis oxaziridine , oxygen , and various peroxyacids (see Rubottom oxidation ).

  8. Bipyridine - Wikipedia

    en.wikipedia.org/wiki/Bipyridine

    Bipyridines are a family of organic compounds with the formula (C 5 H 4 N) 2, consisting of two pyridyl (C 5 H 4 N) rings. Pyridine is an aromatic nitrogen-containing heterocycle. The bipyridines are all colourless solids, which are soluble in organic solvents and slightly soluble in water. Bipyridines, especially the 4,4' isomer, are mainly of ...

  9. Piperidine - Wikipedia

    en.wikipedia.org/wiki/Piperidine

    Piperidine is an organic compound with the molecular formula (CH 2) 5 NH. This heterocyclic amine consists of a six-membered ring containing five methylene bridges (–CH 2 –) and one amine bridge (–NH–).