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  2. 4-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/4-Methylpyridine

    4-Methylpyridine is both isolated from coal tar and is synthesized industrially. It forms via the reaction of acetaldehyde and ammonia in the presence of an oxide catalyst. The method also affords some 2-methylpyridine. 4-Methylpyridine is of little intrinsic value but is a precursor to other commercially significant species, often of medicinal ...

  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. List of branches of psychology - Wikipedia

    en.wikipedia.org/wiki/List_of_branches_of_psychology

    Download as PDF; Printable version ... This non-exhaustive list contains many of the sub-fields within the field of psychology: ... List of branches of psychology.

  5. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1] Heterocyclic organic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of organic heterocycles .

  6. C6H7N - Wikipedia

    en.wikipedia.org/wiki/C6H7N

    4-Methylpyridine Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  7. Transition metal pyridine complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_pyridine...

    trans-[MCl 2 (pyridine) 4] n+ is a common type of transition metal pyridine complex. Chloro(pyridine)cobaloxime. Crabtree's catalyst.. Owing to the relatively wide C-N-C angle, the 2,6-hydrogen atoms interfere with the formation of [M(py) 6] z complexes.

  8. 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 ...

  9. Brooker's merocyanine - Wikipedia

    en.wikipedia.org/wiki/Brooker's_merocyanine

    Brooker's merocyanine (1-methyl-4-[(oxocyclohexadienylidene)ethylidene]-1,4-dihydropyridine, MOED) [1] is an organic dye belonging to the class of merocyanines. MOED is notable for its solvatochromic properties, meaning it changes color depending on the solvent in which it is dissolved.

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