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  2. Azo compound - Wikipedia

    en.wikipedia.org/wiki/Azo_compound

    Azo compounds are organic compounds bearing the functional group diazenyl ( R−N=N−R′, in which R and R′ can be either aryl or alkyl groups). IUPAC defines azo compounds as: "Derivatives of diazene (diimide), HN=NH, wherein both hydrogens are substituted by hydrocarbyl groups, e.g. PhN=NPh azobenzene or diphenyldiazene.", where Ph stands ...

  3. Azo dye - Wikipedia

    en.wikipedia.org/wiki/Azo_dye

    Azo dye. Chemical structure of Solvent Yellow 7, an orange colored azo dye. Azo dyes are organic compounds bearing the functional group R−N=N−R′, in which R and R′ are usually aryl and substituted aryl groups. They are a commercially important family of azo compounds, i.e. compounds containing the C-N=N-C linkage. [ 1]

  4. Azoxy compounds - Wikipedia

    en.wikipedia.org/wiki/Azoxy_compounds

    Azoxy compounds. The structure of the azoxy functional group, where R is a substituent. In chemistry, azoxy compounds are a group of organic compounds sharing a common functional group with the general structure R−N=N+(−O−)−R. [1] They are considered N-oxides of azo compounds. Azoxy compounds are 1,3-dipoles and cycloadd to double bonds.

  5. Azobenzene - Wikipedia

    en.wikipedia.org/wiki/Azobenzene

    Azobenzene is a photoswitchable chemical compound composed of two phenyl rings linked by a N=N double bond. It is the simplest example of an aryl azo compound. The term 'azobenzene' or simply 'azo' is often used to refer to a wide class of similar compounds.

  6. Acid dye - Wikipedia

    en.wikipedia.org/wiki/Acid_dye

    Many blue dyes have this structure as their basic shape. The structure predominates in the leveling class of acid dye. Azo dyes: The structure of azo dyes contains the azo group (R-N=N−R. Most azo dyes are not acid dyes, but many acid dyes are azo dyes. Many acid dyes of the azo type are red in color. [14]

  7. Azo violet - Wikipedia

    en.wikipedia.org/wiki/Azo_violet

    Azo violet ( Magneson I; [ 1] p-nitrobenzeneazoresorcinol) is an azo compound with the chemical formula C 12 H 9 N 3 O 4. It is used commercially as a violet dye and experimentally as a pH indicator, appearing yellow below pH 11, and violet above pH 13. [ 2] It also turns deep blue in the presence of magnesium salt in a slightly alkaline, or ...

  8. Diazo - Wikipedia

    en.wikipedia.org/wiki/Diazo

    Diazo. In organic chemistry, the diazo group is an organic moiety consisting of two linked nitrogen atoms at the terminal position. Overall charge-neutral organic compounds containing the diazo group bound to a carbon atom are called diazo compounds or diazoalkanes[ a] and are described by the general structural formula R2C=N+=N−.

  9. Azo coupling - Wikipedia

    en.wikipedia.org/wiki/Azo_coupling

    Azo coupling. In organic chemistry, an azo coupling is an reaction between a diazonium compound ( R−N≡N+) and another aromatic compound that produces an azo compound ( R−N=N−R’ ). In this electrophilic aromatic substitution reaction, the aryldiazonium cation is the electrophile, and the activated carbon (usually from an arene, which ...