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  2. List of CAS numbers by chemical compound - Wikipedia

    en.wikipedia.org/wiki/List_of_CAS_numbers_by...

    This is a list of CAS numbers by chemical formulas and chemical compounds, indexed by formula.The CAS number is a unique number applied to a specific chemical by the Chemical Abstracts Service (CAS).This list complements alternative listings to be found at list of inorganic compounds and glossary of chemical formulae

  3. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    The systematic name of pyridine, within the Hantzsch–Widman nomenclature recommended by the IUPAC, is azinine. However, systematic names for simple compounds are used very rarely; instead, heterocyclic nomenclature follows historically established common names. IUPAC discourages the use of azinine/azine in favor of pyridine. [128]

  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. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    Although pyridine is an excellent source of carbon, nitrogen, and energy for certain microorganisms, introduction of a halogen moiety significantly retards degradation of the pyridine ring. With the exception of 4-chloropyridine, each of the mono- and di-substituted chloropyridines were found to be relatively resistant to microbiological ...

  7. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    It is the conjugate acid of pyridine. Many related cations are known involving substituted pyridines, e.g. picolines, lutidines, collidines. They are prepared by treating pyridine with acids. [3] As pyridine is often used as an organic base in chemical reactions, pyridinium salts are produced in many acid-base reactions.

  8. Cetylpyridinium chloride - Wikipedia

    en.wikipedia.org/wiki/Cetylpyridinium_chloride

    The name breaks down as: cetyl- refers to the cetyl group, named for its relation to cetyl alcohol, which was first isolated from whale oil (Latin: cetus); [7] pyridinium refers to the cation [C 5 H 5 NH] +, the conjugate acid of pyridine; chloride refers to the anion Cl −.

  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 ...