Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Aldehydes Alizarine

Prenyl-naphthohydroquinone-2-carboxyhc acid is the key intermediate in the formation of anthraquinones of the alizarin type. (In contrast the A-ring-substituted anthraquinone derivatives found in fungi and certain higher plants, e.g., Rhamnaceae and Polygonaceae, are polyketides, D 3.3.5). In the biosynthesis of alizarin one C-atom of the isoprene residue is lost. In structurally related compounds, however, this C-atom may still be present in the form of a methyl, hydroxymethyl, aldehyde, or carboxy group. [Pg.263]

Nitrophenols and nitro-acids, (yellow to orange) salicyl-aldehyde (yellow) derivatives of alizarin JV-bromosucdn-imide phthaleins. [Pg.32]


See other pages where Aldehydes Alizarine is mentioned: [Pg.856]    [Pg.478]    [Pg.1477]    [Pg.237]    [Pg.5389]   
See also in sourсe #XX -- [ Pg.61 ]




SEARCH



Alizarin

© 2024 chempedia.info