| Identification | Back Directory | [Name]
Methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-9-(ethoxymethoxy)-2-(3-furanyl)dodecahydro-6a,10b-dimethyl-4,10-dioxo-2H-naphtho[2,1-c]pyran-7-carboxylate | [CAS]
1017524-76-3 | [Synonyms]
Salvinorin B ethoxymethyl ether
Methyl (2S,4aR,6aR,7R,9S,10aS,10bR)-9-(ethoxymethoxy)-2-(3-furanyl)dodecahydro-6a,10b-dimethyl-4,10-dioxo-2H-naphtho[2,1-c]pyran-7-carboxylate | [Molecular Formula]
C24H32O8 | [MOL File]
1017524-76-3.mol | [Molecular Weight]
448.51 |
| Chemical Properties | Back Directory | [Boiling point ]
567.2±50.0 °C(Predicted) | [density ]
1.24±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted) | [solubility ]
DMF: 20 mg/ml
DMSO: 20 mg/ml
Ethanol: 1 mg/ml |
| Hazard Information | Back Directory | [Description]
Salvinorin B ethoxymethyl ether (Item No. 38171) is an analytical reference standard categorized as a diterpene.1 Salvinorin B ethoxymethyl ether induces stimulus generalization to salvinorin A (Item Nos. 38208 | 11487 | 34779) in rats. This product is intended for research and forensic applications.WARNING This product is not for human or veterinary use. | [References]
[1] MARY MELISSA PEET Lisa E B. Salvinorin B derivatives, EOM-Sal B and MOM-Sal B, produce stimulus generalization in male Sprague-Dawley rats trained to discriminate salvinorin A.[J]. Behavioural Pharmacology, 2011, 22 5-6: 450-457. DOI: 10.1097/fbp.0b013e328349fc1b |
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