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| 16,17-Didehydro-9,17-dihydro-9α-hydroxy-12,13-dimethoxyibogamine-18-carboxylic acid methyl ester Basic information |
Product Name: | 16,17-Didehydro-9,17-dihydro-9α-hydroxy-12,13-dimethoxyibogamine-18-carboxylic acid methyl ester | Synonyms: | 16,17-Didehydro-9,17-dihydro-9α-hydroxy-12,13-dimethoxyibogamine-18-carboxylic acid methyl ester;Jollyanine;Ibogamine-18-carboxylic acid, 16,17-didehydro-9,17-dihydro-9-hydroxy-12,13-dimethoxy-, methyl ester, (9α)- | CAS: | 16671-17-3 | MF: | C23H30N2O5 | MW: | 414.49 | EINECS: | | Product Categories: | | Mol File: | 16671-17-3.mol | ![16,17-Didehydro-9,17-dihydro-9α-hydroxy-12,13-dimethoxyibogamine-18-carboxylic acid methyl ester Structure](CAS/20180808/GIF/16671-17-3.gif) |
| 16,17-Didehydro-9,17-dihydro-9α-hydroxy-12,13-dimethoxyibogamine-18-carboxylic acid methyl ester Chemical Properties |
| 16,17-Didehydro-9,17-dihydro-9α-hydroxy-12,13-dimethoxyibogamine-18-carboxylic acid methyl ester Usage And Synthesis |
Description | Present in Conopharyngia jollyana Stapf., this alkaloid is obtained as colourless
crystals from MeOH and has [α]22D - 56° (c 0.6, CHC13). It contains two
methoxyl groups, one hydroxyl and a C-ethyl group. The ultraviolet spectrum
exhibits absorption maxima at 217,238 and 300 mμ. | References | Hootele et al., Bull. Soc. Chim. Belg., 76,300 (1967) |
| 16,17-Didehydro-9,17-dihydro-9α-hydroxy-12,13-dimethoxyibogamine-18-carboxylic acid methyl ester Preparation Products And Raw materials |
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