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2-Azido-anthraquinone

Azido-Anthraquinone, bright yel ndls (from coned HCOOH), mp 160-162°, turning brown on exposure to light. Defl on heating above the mp. Prepn is described in Refs 1 3... [Pg.459]

Nitro 2 azido-anthraquinone, Pale yel-grn crysts(from pyridine), mp 210° (dec), changing on exposure to light and in the air to pale orange-red (Ref 3). Prepd by rubbing /3-anthraquinone-azide with coned nitric acid... [Pg.460]

The exact location of the functional molecules in these subunits is still rather uncertain. The association of one ubiquinone molecule with the M subunit has been demonstrated by covalent linkage with the photoaffinity-reactive quinone analogue 2-azido-anthraquinone [12]. Similarly the association of the second quinone molecule... [Pg.99]

Nitro-l-azido anthraquinone, yel ndls(from pyridine), mp 245° (dec), expl on rapid heating. Prepd by gentle warming of 4-Nitroanthra-quinonerl-diazohydroxyl amine with acetic anhydride and pyridine (Ref 2)... [Pg.460]

Azidoanthraquinone Fuming HNO3 2-Azido-l-nitro- anthraquinone 27... [Pg.209]

Few investigations have described the photoinduced modification of substrates with the emplo5rfnent of azido- or anthraquinone-derived polymers. [Pg.337]

See other pages where 2-Azido-anthraquinone is mentioned: [Pg.460]    [Pg.460]    [Pg.607]    [Pg.607]    [Pg.111]    [Pg.460]    [Pg.607]    [Pg.607]    [Pg.607]    [Pg.69]   
See also in sourсe #XX -- [ Pg.99 ]



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