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  2. Propanamide - Wikipedia

    en.wikipedia.org/wiki/Propanamide

    This article about an organic compound is a stub. You can help Wikipedia by expanding it.

  3. Propionitrile - Wikipedia

    en.wikipedia.org/wiki/Propionitrile

    Propionitrile is a solvent similar to acetonitrile but with a slightly higher boiling point. It is a precursor to propylamines by hydrogenation. It is a C-3 building block in the preparation of the drug flopropione by the Houben-Hoesch reaction.

  4. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    Ethylamine, also known as ethanamine, is an organic compound with the formula CH 3 CH 2 NH 2.This colourless gas has a strong ammonia-like odor.It condenses just below room temperature to a liquid miscible with virtually all solvents.

  5. 1-Pentyne - Wikipedia

    en.wikipedia.org/wiki/1-Pentyne

    This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it.

  6. Propionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Propionyl_chloride

    Propionyl chloride (also propanoyl chloride) is the organic compound with the formula CH 3 CH 2 C(O)Cl. It is the acyl chloride derivative of propionic acid.It undergoes the characteristic reactions of acyl chlorides. [1]

  7. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O.Commonly abbreviated Ac 2 O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis.

  8. N-Methylmethanimine - Wikipedia

    en.wikipedia.org/wiki/N-Methylmethanimine

    N-Methylmethanimine or N‐methyl methylenimine is a reactive molecular substance containing a methyl group attached to an imine.It can be written as CH 3 N=CH 2.On a timescale of minutes it self reacts to form the trimer trimethyl 1,3,5-triazinane.

  9. Hofmann elimination - Wikipedia

    en.wikipedia.org/wiki/Hofmann_elimination

    Hofmann elimination is an elimination reaction of an amine to form alkenes.The least stable alkene (the one with the fewest substituents on the carbons of the double bond), called the Hofmann product, is formed.