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蒽棓酚

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蒽棓酚
IUPAC名
1,2,3-Trihydroxy-9,10-anthracenedione
1,2,3-三羟基-9,10-蒽二酮
英文名 anthragallol
别名 1,2,3-三羟基蒽醌
识别
CAS号 602-64-2
PubChem 11768
ChemSpider 11275
SMILES
 
  • C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)O)O
InChI
 
  • InChI=1S/C14H8O5/c15-9-5-8-10(14(19)13(9)18)12(17)7-4-2-1-3-6(7)11(8)16/h1-5,15,18-19H
InChIKey AHKDJQYHVWSRLT-UHFFFAOYSA-N
ChEBI 2755
性质
化学式 C14H8O5
摩尔质量 256.21 g·mol−1
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

蒽棓酚(英语:anthragallol)是一种有机化合物,化学式C14H8O5,可见于染色茜草[1][2]Coprosma lucida英语Coprosma lucida[3][4]毛土连翘[5]等物种。

参考资料

[编辑]
  1. ^ K. Krizsán; Gy. Szókán; Z. A. Toth; F. Hollósy; M. László; A. Khlafulla. HPLC Analysis of Anthraquinone Derivatives in Madder Root (Rubia Tinctorum) and Its Cell Cultures. Journal of Liquid Chromatography and Related Technologies. 2007-07, 19 (14). doi:10.1080/10826079608017158. 
  2. ^ A. R. Burnett; R. H. Thomson. Naturally occurring quinones. Part XV. Biogenesis of the anthraquinones in Rubia tinctorum L. (madder). Journal of the Chemical Society. C.Organic. 1968. doi:10.1039/J39680002437. 
  3. ^ Lindsay H. Briggs; G. A. Nicholls. 611. Chemistry of the Coprosma genus. Part VII. A revised constitution for lucidin. Journal of the Chemical Society. 2004-04. doi:10.1039/JR9530003068. 
  4. ^ Lindsay H. Briggs; G. A. Nicholls. 269. Chemistry of the coprosma genus. Part IV. The non-glycosidic anthraquinone compounds from coprosma lucida. Journal of the Chemical Society. 1949. doi:10.1039/JR9490001241. 
  5. ^ E. J. C. Brew; R. H. Thomason. Naturally occurring quinones. Part XIX. Anthraquinones in hymenodictyon excelsum and damnacanthus major. Journal of the Chemical Society. C.Organic. 1971. doi:10.1039/J39710002001.