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| 20-Ethyl-1α,16β-dimethoxy-4-[[[2-(acetylamino)benzoyl]oxy]methyl]aconitane-8,14α-diol Basic information |
Product Name: | 20-Ethyl-1α,16β-dimethoxy-4-[[[2-(acetylamino)benzoyl]oxy]methyl]aconitane-8,14α-diol | Synonyms: | 20-Ethyl-1α,16β-dimethoxy-4-[[[2-(acetylamino)benzoyl]oxy]methyl]aconitane-8,14α-diol;Aconorine;Aconitane-8,14-diol, 4-[[[2-(acetylamino)benzoyl]oxy]methyl]-20-ethyl-1,16-dimethoxy-, (1α,14α,16β)- | CAS: | 58969-45-2 | MF: | C32H44N2O7 | MW: | 568.7 | EINECS: | | Product Categories: | | Mol File: | 58969-45-2.mol | |
| 20-Ethyl-1α,16β-dimethoxy-4-[[[2-(acetylamino)benzoyl]oxy]methyl]aconitane-8,14α-diol Chemical Properties |
Boiling point | 736.8±60.0 °C(Predicted) | density | 1.33±0.1 g/cm3(Predicted) | pka | 13.57±0.70(Predicted) |
| 20-Ethyl-1α,16β-dimethoxy-4-[[[2-(acetylamino)benzoyl]oxy]methyl]aconitane-8,14α-diol Usage And Synthesis |
Description | Anum ber of A coni tum species elaborate this alkaloid which has been shown to
possess the structure given above, based primarily upon infrared, NMR and mass
spectroscopic studies. Saponification of the base yields columbianine. | References | Tel'nov et al., Khim. Prir. Soedin., 11,814 (1975) |
| 20-Ethyl-1α,16β-dimethoxy-4-[[[2-(acetylamino)benzoyl]oxy]methyl]aconitane-8,14α-diol Preparation Products And Raw materials |
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