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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. 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)−.

  4. Dimethylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylbenzylamine

    Other names N,N-Dimethylbenzenemethanamine, ... N,N-Dimethylbenzylamine can be synthesized by the Eschweiler–Clarke reaction of benzylamine [2] [3] Reactions

  5. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    ChemAxon Name <> Structure – ChemAxon IUPAC (& traditional) name to structure and structure to IUPAC name software. As used at chemicalize.org; chemicalize.org A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched.

  6. Duff reaction - Wikipedia

    en.wikipedia.org/wiki/Duff_reaction

    Protonated hexamine ring-opens to expose an iminium group. Addition to the aromatic ring results in an intermediate at the oxidation state of a benzylamine. An intramolecular redox reaction then ensues, raising the benzylic carbon to the oxidation state of an aldehyde. The oxygen atom is provided by water on acid hydrolysis in the final step.

  7. 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).

  8. 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.

  9. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    Some element names were new and received English versions similar to the French names. [22] For the new "element" caloric, both the new and some of the "old" names (igneous fluid and matter of fire and of heat) were coined by Lavoisier, their discoverer. Most element names, however, were not new, so they retained their existing English versions.