Hydroxyanthraquinone

A hydroxyanthraquinone (formula: C14H9O2(OH)) is any of several organic compounds that can be viewed as derivatives of an anthraquinone through replacement of one hydrogen atom (H) by an hydroxyl group (-OH). The IUPAC nomenclature recommends hydroxyanthracenedione.

Usually "hydroxyanthraquinone" refers to a derivative of 9,10-anthraquinone.[1][2][3]

Isomers

In general, the term may mean any anthraquinone derivative where any number n of hydrogens have been replaced by n hydroxyls, so that the formula is C
14H
10O
2+n. In this case, the number n (which is between 1 and 8) is indicated by a multiplier prefix (mono-, di-, tri-, up to octa-). Additional hydroxy- compounds can be derived from the other isomers of the latter. From 9,10-anthraquinone, only two single-hydroxy derivatives are possible.

See also

References

  1. ↑ Khalafy, J.; Bruce, J. M. (2002). "Oxidative Dehydrogenation of 1-Tetralones: Synthesis of Juglone, Naphthazarin, and α-Hydroxyanthraquinones" (pdf). Journal of Sciences, Islamic Republic of Iran. 13 (2): 131–139.
  2. ↑ Thomson, R. H. (1971). Naturally Occurring Quinones. London: Academic Press. Quoted by Khalafy and Bruce.
  3. ↑ Thomson, R. H. (1987). Naturally Occurring Quinones III. London: Chapman and Hall. Quoted by Khalafy and Bruce.
This article is issued from Wikipedia - version of the 5/31/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.