pyridine in A Sentence

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    Formation of pyridinium through elimination reaction with Pyridine.

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    Pyridine is Density 0.978 g/ cm3. Flash point 68°F.

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    Pyridine is used to dissolve other substances.

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    Pyridine hydrochloride synthesis,

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    Pharmaceutically useful Pyridines.

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    Pyrazine is less basic than Pyridine, pyridazine and pyrimidine.

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    In condensation reactions, Pyridine is typically applied as a base.

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    This product is an organic chemical under the class of Pyridines.

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    In acylations and esterifications, Pyridine activates the anhydrides or carboxylic acid halides.

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    Direct nitration is considered to be more comfortable than direct sulfonation of Pyridine.

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    Pyridine is a clear liquid with an odor that is sour, putrid, and fish-like.

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    The final process is an oxidation reaction with a solid-state catalyst to yield Pyridine.

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    Abramovitch, John Wiley & Sons, Pyridine and Its Derivatives, Supplement 17 Sep 2009, Science, page 1002-1005.

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    Pyridines are heterocyclic compounds which are used to dissolve other substances to make various products such as;

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    Pyridinium chlorochromate is customarily obtained when Pyridine is added to the solution of concentrated hydrochloric and chromic acid.

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    Abramovitch, John Wiley & Sons, 22 Feb 197, Heterocyclic compounds, The Chemistry of Heterocyclic Compounds, Pyridine and Its Derivatives: Supplement.

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    In addition, both oxygen and nitrogen heterocyclic hydrocarbons, such as parent and alkyl homologues of carbazole, quinoline, and Pyridine, are present in many crude oils.

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    18

    The use of strong alkalines such as sodium and potassium tert-butoxide can help to get rid of Pyridine derivatives when using the right leaving the group.

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