| Company Name: |
BOC Sciences |
| Tel: |
+1-631-485-4226 |
| Email: |
inquiry@bocsci.com |
|
| | Chevalone E Basic information |
| Product Name: | Chevalone E | | Synonyms: | Chevalone E;1H,11H-Phenanthro[2,1-b]pyrano[3,2-e]pyran-11-one, 2,3,4,4a,4b,5,6,6a,12,12a,12b,13,14,14a-tetradecahydro-2-hydroxy-1,1,4a,6a,9,12b-hexamethyl-, (2S,4aR,4bR,6aS,12aS,12bR,14aR)-;(2S,4aR,4bR,6aS,12aS,12bR,14aR)-2,3,4,4a,4b,5,6,6a,12,12a,12b,13,14,14a-tetradecahydro-2-hydroxy-1,1,4a,6a,9,12b-hexamethyl-1H,11H-phenanthro[2,1-b]pyrano[3,2-e]pyran-11-one | | CAS: | 1315451-94-5 | | MF: | C26H38O4 | | MW: | 414.58 | | EINECS: | | | Product Categories: | | | Mol File: | 1315451-94-5.mol |  |
| | Chevalone E Chemical Properties |
| Boiling point | 532.1±50.0 °C(Predicted) | | density | 1.16±0.1 g/cm3(Predicted) | | solubility | DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble | | form | A solid | | pka | 15.16±0.70(Predicted) |
| | Chevalone E Usage And Synthesis |
| Description | Chevalone E is a meroterpene that has been found in A. similanensis.1 | | References | 1. Prompanya, C., Dethoup, T., Bessa, L.J., et al. New isocoumarin derivatives and meroterpenoids from the marine sponge-associated fungus Aspergillus similanensis sp. nov. KUFA 0013 Mar. Drugs 12(10),5160-5173(2014). |
| | Chevalone E Preparation Products And Raw materials |
|