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  2. Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/Nitroaniline

    The term nitroaniline in chemistry refers to a derivative of aniline (C 6 H 5 NH 2) containing a nitro group (—NO 2) There are three simple nitroanilines of formula C 6 H 4 (NH 2)(NO 2) which differ only in the position of the nitro group: 2-Nitroaniline; 3-Nitroaniline; 4-Nitroaniline

  3. 3-Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/3-Nitroaniline

    3-Nitroaniline is an organic compound with the formula H 2 NC 6 H 4 NO 2. A yellow solid, it is a derivative of aniline, carrying a nitro functional group in position 3. It is an isomer of 2-nitroaniline and 4-nitroaniline. It is used as a precursor to dyes. [1]

  4. 4-Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/4-Nitroaniline

    4-Nitroaniline, p-nitroaniline or 1-amino-4-nitrobenzene is an organic compound with the formula C 6 H 6 N 2 O 2. A yellow solid, it is one of three isomers of nitroaniline. It is an intermediate in the production of dyes, antioxidants, pharmaceuticals, gasoline, gum inhibitors, poultry medicines, and as a corrosion inhibitor. [3]

  5. 2-Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/2-Nitroaniline

    2-Nitroaniline is an organic compound with the formula H 2 NC 6 H 4 NO 2. It is a derivative of aniline , carrying a nitro functional group in position 2. [ 1 ] It is mainly used as a precursor to o-phenylenediamine.

  6. 1,3-Dinitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,3-Dinitrobenzene

    Reduction of 1,3-dinitrobenzene with sodium sulfide in aqueous solution leads to 3-nitroaniline. Further reduction with iron and hydrochloric acid (HCl) gives m-phenylenediamine. [2] 1,3-Dinitrobenzene can be nitrated to 1,3,5-trinitrobenzene with nitronium tetrafluoroborate in fluorosulfuric acid at 150 °C. [3] [4]

  7. 2-Methoxy-4-nitroaniline - Wikipedia

    en.wikipedia.org/wiki/2-Methoxy-4-nitroaniline

    2-Methoxy-4-nitroaniline is an organic compound with the formula O 2 NC 6 H 3 (OCH 3)NH 2. [2] It is one of four isomers of methoxynitroaniline. The compound is a precursor to the commercial Pigment Yellow 74 .

  8. Nitroamine - Wikipedia

    en.wikipedia.org/wiki/Nitroamine

    N-Nitroaniline rearranges in the presence of acid to give 2-nitroaniline. [4] References Further reading. Schmidt, Eckart W. (2022). "Nitramines". ...

  9. 2,4-Dinitroaniline - Wikipedia

    en.wikipedia.org/wiki/2,4-dinitroaniline

    4,800 m/s Hazards Occupational ... 4-Nitroaniline. Except where otherwise noted, ... 2,4-Dinitroaniline is a chemical compound with a formula of C 6 H 5 N 3 O 4.