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  2. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2). It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group , NH 2 .

  3. Open Notebook Science Challenge - Wikipedia

    en.wikipedia.org/wiki/Open_Notebook_Science...

    The Open Notebook Science Challenge is a crowdsourcing research project which collects measurements of the non-aqueous solubility of organic compounds and publishes these as open data; findings are reported in an open notebook science manner. Although anyone may contribute research data, the competition is only open to post-secondary students ...

  4. Dibenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dibenzylamine

    Dibenzylamine is an organic compound with the formula (C 6 H 5 CH 2) 2 NH.It is classified as a secondary amine, being the middle member of the series that includes the primary amine benzylamine (C 6 H 5 CH 2 NH 2) and the tertiary amine tribenzylamine ((C 6 H 5 CH 2) 3 N).

  5. Dimethylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylbenzylamine

    Download as PDF; Printable version ... Solubility in water. 1.2 g/100mL ... N,N-Dimethylbenzylamine can be synthesized by the Eschweiler–Clarke reaction of ...

  6. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/100 ml), unless shown otherwise. The substances are listed in alphabetical order.

  7. Isopropylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Isopropylbenzylamine

    N-isopropylbenzylamine is a compound that has appeared in chemical literature often playing an intermediary role in applications of experimental synthesis and novel organic transformations.

  8. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl is most commonly abbreviated Bn. For example, benzyl alcohol can be represented as BnOH. Less common abbreviations are Bzl and Bz, the latter of which is ambiguous as it is also the standard abbreviation for the benzoyl group C 6 H 5 C(O)−.

  9. 1-Phenylethylamine - Wikipedia

    en.wikipedia.org/wiki/1-Phenylethylamine

    1-Phenylethylamine may be prepared by the reductive amination of acetophenone: [1]. C 6 H 5 C(O)CH 3 + NH 3 + H 2 → C 6 H 5 CH(NH 2)CH 3 + H 2 O. The Leuckart reaction, using ammonium formate, is another method for this transformation.