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  2. 4-Dimethylaminopyridine - Wikipedia

    en.wikipedia.org/wiki/4-Dimethylaminopyridine

    4-Dimethylaminopyridine (DMAP) is a derivative of pyridine with the chemical formula (CH 3) 2 NC 5 H 4 N. This white solid is of interest because it is more basic than pyridine , owing to the resonance stabilisation from the NMe 2 substituent.

  3. 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]

  4. Pyridinium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_p-toluenesulfonate

    In organic synthesis, PPTS is used as a weakly acidic catalyst, providing an organic soluble source of pyridinium (C 5 H 5 NH +) ions.For example, PPTS is used to deprotect silyl ethers or tetrahydropyranyl ethers when a substrate is unstable to stronger acid catalysts.

  5. 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 ...

  6. 4-Aminopyridine - Wikipedia

    en.wikipedia.org/wiki/4-Aminopyridine

    4-Aminopyridine is also used under the trade name Avitrol as 0.5% or 1% in bird control bait. It causes convulsions and, infrequently, death, depending on dosage. [18] The manufacturer says the proper dose should cause epileptic-like convulsions which cause the poisoned birds to emit distress calls resulting in the flock leaving the site; if the dose was sub-lethal, the birds will recover ...

  7. 2-Methyleneglutaronitrile - Wikipedia

    en.wikipedia.org/wiki/2-Methyleneglutaronitrile

    2-Methylenglutaronitrile reacts with methanamide upon catalysis with 4-(dimethylamino)-pyridine (DMAP) at 60 °C in 47% yield to give 1-(N-methanoylamino)-2,4-dicyanobutane, from which α- aminomethylglutaric acid is formed by subsequent hydrolysis. [14] Reaktion von 2-Methylenglutaronitril mit Formamid zu 1-(N-Formylamino)-2,4-dicyanobutan

  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. Chloro(pyridine)cobaloxime - Wikipedia

    en.wikipedia.org/wiki/Chloro(pyridine)cobaloxime

    Chloro(pyridine)cobaloxime(III) is first reduced to Chloro(pyridine)cobaloxime(I) by sodium borohydride in alkaline solution, then an alkyl halide is added into the reaction mixture, and the desired Co-C bond is formed via a S N 2 reaction. This method can be used to produce cobaloximes containing a primary or a secondary alkyl substituent.