2(4H)-Benzofuranone, 6-ethenyl-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-5-(1-methylethenyl)-, (5S,6S,7aS)- manufacturers
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| | 2(4H)-Benzofuranone, 6-ethenyl-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-5-(1-methylethenyl)-, (5S,6S,7aS)- Basic information |
| Product Name: | 2(4H)-Benzofuranone, 6-ethenyl-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-5-(1-methylethenyl)-, (5S,6S,7aS)- | | Synonyms: | 2(4H)-Benzofuranone, 6-ethenyl-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-5-(1-methylethenyl)-, (5S,6S,7aS)-;Hydroxyisogermafurenolide, 10 mM in DMSO;Hydroxyisogermafurenolide | | CAS: | 20267-91-8 | | MF: | C15H20O3 | | MW: | 248.32 | | EINECS: | | | Product Categories: | | | Mol File: | 20267-91-8.mol |  |
| | 2(4H)-Benzofuranone, 6-ethenyl-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-5-(1-methylethenyl)-, (5S,6S,7aS)- Chemical Properties |
| Boiling point | 401.7±45.0 °C(Predicted) | | density | 1.10±0.1 g/cm3(Predicted) | | pka | 10.62±0.70(Predicted) |
| | 2(4H)-Benzofuranone, 6-ethenyl-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-5-(1-methylethenyl)-, (5S,6S,7aS)- Usage And Synthesis |
| Uses | Hydroxyisogermafurenolide is a lactone isolated from the root of Nux vomica[1]. | | References | [1] Takeda K, et al. Components of the root of Lindera strychnifolia Vill. Part XIV. Sesquiterpene lactones from the root of Lindera strychnifolia Vill[J]. Journal of the Chemical Society C: Organic, 1968: 569-572. |
| | 2(4H)-Benzofuranone, 6-ethenyl-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-5-(1-methylethenyl)-, (5S,6S,7aS)- Preparation Products And Raw materials |
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