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  2. Aniline - Wikipedia

    en.wikipedia.org/wiki/Aniline

    Aniline (from Portuguese anil 'indigo shrub', and -ine indicating a derived substance) [6] is an organic compound with the formula C 6 H 5 NH 2. Consisting of a phenyl group ( −C 6 H 5 ) attached to an amino group ( −NH 2 ), aniline is the simplest aromatic amine .

  3. Anilinium chloride - Wikipedia

    en.wikipedia.org/wiki/Anilinium_chloride

    A white solid, it is the chloride salt of anilinium, which is the conjugate acid of aniline, C 6 H 5 NH 2. Anilinium chloride is produced by treatment of aniline with hydrochloric acid. The cation consists of a phenyl ring attached to a tetrahedral ammonium center. The C-N bond elongates from 1.41 Å in aniline to 1.474 Å in anilinium. [2]

  4. Aniline (data page) - Wikipedia

    en.wikipedia.org/wiki/Aniline_(data_page)

    Aniline absorbs in the K (220 - 250 nm) and the B (250 - 290 nm) bands exhibited by benzenoid compounds. The K and B bands arise from π to π* transitions as a result of the a group containing multiple bond being attached to the benzene ring. When dissolved in ethanol, λ max for aniline is 230 nm, but in dilute aqueous acid λ max is 203 nm ...

  5. Dimethylaniline - Wikipedia

    en.wikipedia.org/wiki/Dimethylaniline

    N,N-Dimethylaniline (DMA) is an organic chemical compound, a substituted derivative of aniline. It is a tertiary amine, featuring a dimethylamino group attached to a phenyl group. This oily liquid is colourless when pure, but commercial samples are often yellow. It is an important precursor to dyes such as crystal violet.

  6. Dichloroaniline - Wikipedia

    en.wikipedia.org/wiki/Dichloroaniline

    Dichloroanilines are chemical compounds which consist of an aniline ring substituted with two chlorine atoms and have the molecular formula C 6 H 5 Cl 2 N. There are six isomers, varying in the positions of the chlorine atoms around the ring relative to the amino group. As aniline derivatives, they are named with the amino group in position 1.

  7. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    The hydrochloride salt of benzylamine, C 6 H 5 CH 2 NH 3 Cl or C 6 H 5 CH 2 NH 2 ·HCl, [24] is prepared by reacting benzylamine with hydrochloric acid, and can be used in treating motion sickness. NASA astronaut John Glenn was issued with benzylamine hydrochloride for this purpose for the Mercury-Atlas 6 mission. [ 25 ]

  8. Anilide - Wikipedia

    en.wikipedia.org/wiki/Anilide

    General structure of an anilide, where R denotes possible substituents. In organic chemistry, anilides (or phenylamides) are a class of organic compounds with the general structure R−C(=O)−N(−R’)−C 6 H 5. They are amide derivatives of aniline (H 2 N−C 6 H 5).

  9. Fuchsine - Wikipedia

    en.wikipedia.org/wiki/Fuchsine

    Fuchsine (sometimes spelled fuchsin) or rosaniline hydrochloride is a magenta dye with chemical formula C 20 H 19 N 3 ·HCl. [1] [2] There are other similar chemical formulations of products sold as fuchsine, and several dozen other synonyms of this molecule. [1] It becomes magenta when dissolved in water; as a solid, it forms dark green crystals.