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  2. Dimethylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylbenzylamine

    Dimethylbenzylamine is the organic compound with the formula C 6 H 5 CH 2 N(CH 3) 2. The molecule consists of a benzyl group, C 6 H 5 CH 2, attached to a dimethylamino functional group. It is a colorless liquid. It is used as a catalyst for the formation of polyurethane foams and epoxy resins.

  3. N,N-Dimethylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Dimethylethylamine

    N,N-Dimethylethylamine (DMEA), sometimes referred to as dimethylethylamine, is an organic compound with formula (CH 3) 2 NC 2 H 5.It is an industrial chemical that is mainly used in foundries as a catalyst for epoxy resins and polyurethane as well as sand core production.

  4. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine is used as a masked source of ammonia, since after N-alkylation, the benzyl group can be removed by hydrogenolysis: [10] C 6 H 5 CH 2 NH 2 + 2 RBr → C 6 H 5 CH 2 NR 2 + 2 HBr C 6 H 5 CH 2 NR 2 + H 2 → C 6 H 5 CH 3 + R 2 NH. Typically a base is employed in the first step to absorb the HBr (or related acid for other kinds of ...

  5. Berberine, a plant compound traditionally used in herbal medicine, is today commonly stocked on the shelves of health food stores and pharmacies as a supplement.. Berberine supplements gained ...

  6. Sommelet–Hauser rearrangement - Wikipedia

    en.wikipedia.org/wiki/Sommelet–Hauser...

    The Sommelet–Hauser rearrangement (named after M. Sommelet [1] and Charles R. Hauser [2]) is a rearrangement reaction of certain benzyl quaternary ammonium salts. [3] [4] The reagent is sodium amide or another alkali metal amide and the reaction product a N,N-dialkylbenzylamine with a new alkyl group in the aromatic ortho position.

  7. N,N'-Dimethylethylenediamine - Wikipedia

    en.wikipedia.org/wiki/N,N'-Dimethylethylenediamine

    N,N'-Dimethylethylenediamine (DMEDA) is the organic compound with the formula (CH 3 NH) 2 C 2 H 4. It is a colorless liquid with a fishy odor. It features two secondary amine functional groups. Regarding its name, N and N' indicate that the methyl groups are attached to different nitrogen atoms.

  8. Charles R. Hauser - Wikipedia

    en.wikipedia.org/wiki/Charles_R._Hauser

    [6] [7] The reagent is sodium amide or another alkali metal amide and the reaction product a N,N-dialkylbenzylamine with a new alkyl group in the aromatic ortho position. For example, benzyltrimethylammonium iodide, [(C 6 H 5 CH 2)N(CH 3) 3]I, rearranges in the presence of sodium amide to yield the o-methyl derivative of N,N-dimethylbenzylamine ...

  9. Lauryldimethylamine oxide - Wikipedia

    en.wikipedia.org/wiki/Lauryldimethylamine_oxide

    Lauryldimethylamine oxide (LDAO), also known as dodecyldimethylamine oxide (DDAO), is an amine oxide–based zwitterionic surfactant, with a C 12 (dodecyl) alkyl tail. It is one of the most frequently-used surfactants of this type. [4]