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  2. Aliphatic amine - Wikipedia

    en.wikipedia.org/?title=Aliphatic_amine&redirect=no

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  3. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  4. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compounds can be saturated, joined by single bonds (), or unsaturated, with double bonds or triple bonds ().If other elements (heteroatoms) are bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine, it is no longer a hydrocarbon, and therefore no longer an aliphatic compound.

  5. Zincke reaction - Wikipedia

    en.wikipedia.org/wiki/Zincke_reaction

    With secondary amines and not primary amines the Zincke reaction takes on a different shape forming so-called Zincke aldehydes in which the pyridine ring is ring-opened with the terminal iminium group hydrolyzed to an aldehyde: [4] Zincke aldehydes. This variation has been applied in the synthesis of novel indoles: [11] Zincke aldehydes Kearney ...

  6. Category:Amines - Wikipedia

    en.wikipedia.org/wiki/Category:Amines

    العربية; Azərbaycanca; বাংলা; Башҡортса; Беларуская; Беларуская (тарашкевіца) Български

  7. Alkylamines - Wikipedia

    en.wikipedia.org/wiki/Alkylamines

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  8. 2-Naphthylamine - Wikipedia

    en.wikipedia.org/wiki/2-Naphthylamine

    When reduced by sodium in boiling amyl alcohol solution, it forms tetrahydro-3-naphthylamine, which exhibits the properties of the aliphatic amines in that it is strongly alkaline in reaction, has an ammoniacal odor and cannot be diazotized. On oxidation, it yields ortho-carboxy-hydrocinnamic acid, HO 2 CC 6 H 4 CH 2 CH 2 CO 2 H.

  9. Vinyl sulfone dyes - Wikipedia

    en.wikipedia.org/wiki/Vinyl_sulfone_dyes

    If the vinyl sulfone group is introduced via a primary or secondary aliphatic amine, this is performed again by condensation with a halotriazine compound. An example is 2-[2-(2-chlorethylsulfonyl)ethoxy]ethanamine used in bifunctional reactive dyes in combination with a monofluoro or monochlorotriazine hook.