3,6,8-Trihydroxy-1-methylxanthone manufacturers
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| | 3,6,8-Trihydroxy-1-methylxanthone Basic information |
| Product Name: | 3,6,8-Trihydroxy-1-methylxanthone | | Synonyms: | 1,3,6-Trihydroxy-8-methyl-9H-xanthen-9-one;3,6,8-Trihydroxy-1-methylxanthone;rlichexanthone;Fusarindin;9H-Xanthen-9-one, 1,3,6-trihydroxy-8-methyl-;Norlichexanthone | | CAS: | 20716-98-7 | | MF: | C14H10O5 | | MW: | 258.23 | | EINECS: | | | Product Categories: | | | Mol File: | 20716-98-7.mol |  |
| | 3,6,8-Trihydroxy-1-methylxanthone Chemical Properties |
| Melting point | 226-228 °C | | Boiling point | 567.8±49.0 °C(Predicted) | | density | 1.563±0.06 g/cm3(Predicted) | | pka | 6.83±0.20(Predicted) |
| | 3,6,8-Trihydroxy-1-methylxanthone Usage And Synthesis |
| Uses | Norlichexanthone is a compound isolated from the stem bark of Kandelia candel (L.) Druce, Rhizophoraceae[1]. | | Definition | ChEBI: A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 6 and a methyl group at position 8. It has been isolated from | | References | [1] Liu F, et al. The bioactive metabolites of the mangrove endophytic fungus Talaromyces sp. ZH-154 isolated from Kandelia candel (L.) Druce [published correction appears in Planta Med. 2010 Jan;76(2):e9]. Planta Med. 2010;76(2):185-189. DOI:10.1055/s-0029-1186047 |
| | 3,6,8-Trihydroxy-1-methylxanthone Preparation Products And Raw materials |
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