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  2. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Pyridine is a basic heterocyclic organic compound with the chemical formula C 5 H 5 N.It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−).

  3. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    Pyrithione, the conjugate base of 2-mercaptopyridine-N-oxide, is a fungicide found in some shampoos. Oxidation 2-chloropyridine gives 2-chloropyridine-N-oxide. [ 5 ] The antihistamine pheniramine may be generated via the reaction of phenylacetonitrile with 2-chloropyridine in the presence of a base.

  4. Pyridine (data page) - Wikipedia

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

    Phase behavior Triple point: 231.48 K (–41.67 °C), ? Pa Critical point: 619 K (346 °C), 5660 Pa Std enthalpy change of fusion, Δ fus H o: 8.28 kJ/mol Std entropy change

  5. Pyridinium chloride - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chloride

    Containing a pyridinium ion, pyridinium chloride has a pK a of approximately 5, slightly more acidic than that of typical amines.This is due to the hybridization of the nitrogen: the nitrogen is sp 2 hybridized and more electronegative than those nitrogens in ammonium cations, which are sp 3 hybridized.

  6. Picolinic acid - Wikipedia

    en.wikipedia.org/wiki/Picolinic_acid

    Picolinic acid is an organic compound with the formula NC 5 H 4 CO 2 H.It is a derivative of pyridine with a carboxylic acid (COOH) substituent at the 2-position. It is an isomer of nicotinic acid and isonicotinic acid, which have the carboxyl side chain at the 3- and 4-positions, respectively.

  7. 2,4,6-Trimethylpyridine - Wikipedia

    en.wikipedia.org/wiki/2,4,6-trimethylpyridine

    2,4,6-Trimethylpyridine (2,4,6-collidine) is an organic compound which belongs to the heterocycles (more precisely, heteroaromatics).It consists of a pyridine ring substituted with three methyl groups.

  8. Piperidine - Wikipedia

    en.wikipedia.org/wiki/Piperidine

    The name comes from the genus name Piper, which is the Latin word for pepper. [7] Although piperidine is a common organic compound, it is best known as a representative structure element within many pharmaceuticals and alkaloids , such as natural-occurring solenopsins .

  9. Pyridinium chlorochromate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chlorochromate

    C 5 H 5 N + HCl + CrO 3 → [C 5 H 5 NH][CrO 3 Cl] In one alternative method, formation of toxic chromyl chloride (CrO 2 Cl 2) fumes during the making of the aforementioned solution were minimized by simply changing the order of addition: a cold solution of pyridine in concentrated hydrochloric acid was added to solid chromium trioxide under ...