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| | Gymnomitrol Basic information |
| Product Name: | Gymnomitrol | | Synonyms: | (3aS,9S)-Decahydro-3aβ,4,8aβ-trimethyl-7-methylene-4β,8β-methanoazulen-9-ol;Gymnomitrol;4,8-Methanoazulen-9-ol, decahydro-3a,4,8a-trimethyl-7-methylene-, (3aS,4S,8R,8aS,9S)- | | CAS: | 41410-53-1 | | MF: | C15H24O | | MW: | 220.35 | | EINECS: | | | Product Categories: | | | Mol File: | 41410-53-1.mol |  |
| | Gymnomitrol Chemical Properties |
| Boiling point | 289.1±9.0 °C(Predicted) | | density | 1.02±0.1 g/cm3(Predicted) | | pka | 14.72±0.70(Predicted) |
| | Gymnomitrol Usage And Synthesis |
| Description | Gymnomitrol, a novel tricyclic sesquiterpenoid alcohol from the liverwort Gymnomitrion obtusum(Lindb) Pears, is formulated on chemical and spectroscopic evidence and the novel carbon skeleton is shown to be derivable biogenetically from γ-bisabolene via a trichodiene intermediate.[1] | | Synthesis | The tricyclic sesquiterpenoid gymnomitrol was isolated as a major metabolite from liverwort Gymnomitrion obtusum (Lindb.) Pears. The corresponding hydrocarbon, gymnomitrene (previously known as P-barbatene2 or P-pompene3), also occurs with gymnomitrol. The structure and stereochemistry of gymnomitrol were determined by degradation and spectroscopy in conjunction with biogenetic considerations. The unique carbon framework of this cyclotrichothecane is thought to arise, biogenetically, from bazzanene.
 | | References | [1] J. D. CONNOLLY Ian M S T A E Harding. Gymnomitrol, a novel tricyclic sesquiterpenoid from Gymnomitrion obtusum(Lindb) Pears (hepaticae)[J]. Journal of The Chemical Society, Chemical Communications, 1972, 42 1: 1320-1321. DOI:10.1039/C39720001320.
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| | Gymnomitrol Preparation Products And Raw materials |
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