| 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（英語：anthragallol）是一种有机化合物，化学式C14H8O5，可见于染色茜草[1][2]、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.
