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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. 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 ...

  4. 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.

  5. 3-hydroxy-2-methylpyridine-4,5-dicarboxylate 4-decarboxylase

    en.wikipedia.org/wiki/3-hydroxy-2-methylpyridine...

    The systematic name of this enzyme class is 3-hydroxy-2-methylpyridine-4,5-dicarboxylate 4-carboxy-lyase (3-hydroxy-2-methylpyridine-5-carboxylate-forming). This enzyme is also called 3-hydroxy-2-methylpyridine-4,5-dicarboxylate 4-carboxy-lyase. This enzyme participates in vitamin B 6 metabolism.

  6. Nucleotide base - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_base

    It differs in having an extra amine group, creating a more stable bond to thymine. [3] Adenine and guanine have a fused-ring skeletal structure derived of purine, hence they are called purine bases. [4] The purine nitrogenous bases are characterized by their single amino group (−NH 2), at the C6 carbon in adenine and C2 in guanine. [5]

  7. Pyrimidine - Wikipedia

    en.wikipedia.org/wiki/Pyrimidine

    Pyrimidine (C 4 H 4 N 2; / p ɪ ˈ r ɪ. m ɪ ˌ d iː n, p aɪ ˈ r ɪ. m ɪ ˌ d iː n /) is an aromatic, heterocyclic, organic compound similar to pyridine (C 5 H 5 N). [3] One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has nitrogen atoms at positions 1 and 3 in the ring.

  8. 5-pyridoxate dioxygenase - Wikipedia

    en.wikipedia.org/wiki/5-pyridoxate_dioxygenase

    The 4 substrates of this enzyme are 3-hydroxy-4-hydroxymethyl-2-methylpyridine-5-carboxylate, NADPH, H +, and O 2, whereas its two products are 2-(acetamidomethylene)-3-(hydroxymethyl)succinate and NADP +.

  9. 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.