| Weight | 196.205 g/mol |
|---|---|
| Formula | C13H8O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
XANTHONE (90-47-1)
xanthen-9-one · 9-Oxoxanthene
Score:
#2507 in Biochemistry
,
#4894 in Biology
,
#6264 in Chemistry
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- Xanthone Derivatives: New Insights in Biological Activities (Current Medicinal Chemistry, 2005)
- Solvent effects in the photochemistry of xanthone (Journal of the American Chemical Society, 1980)
- Screening of Mango (Mangifera indica L.) Cultivars for Their Contents of Flavonol O- and Xanthone C-Glycosides, Anthocyanins, and Pectin (Journal of Agricultural and Food Chemistry, 2005)
- Identification of flavonol and xanthone glycosides from mango (Mangifera indica L. Cv. Tommy Atkins ) peels by high-performance liquid chromatography-electrospray ionization mass spectrometry (Journal of Agricultural and Food Chemistry, 2003)
- Antidiabetic activity of a xanthone compound, mangiferin (Phytomedicine, 2001)
- Bis(DpaZnII) Appended Xanthone: Excitation Ratiometric Chemosensor for Phosphate Anions (Angewandte Chemie, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - xanthen-9-one
- 9-Oxoxanthene
-
SMILESC1=CC=C2C(=C1)C(=O)C3=CC=CC=C3O2
-
InChIKeyJNELGWHKGNBSMD-UHFFFAOYSA-N
- Pubchem - XANTHONE
- Wikipedia - xanthone
Xanthone is an organic compound with the molecular formula C13H8O2. It can be prepared by the heating of phenyl salicylate. In 1939, xanthone was introduced as an insecticide and it currently finds uses as ovicide for codling moth eggs and as a larvicide.
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