蒽棓酚

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

^ 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.
^ 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.
^ 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.
^ 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.
^ 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.

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