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| (5α,12β,19α,20R)-2,3-Didehydro-16-methoxy-20-[[(7-methoxy-1,3-benzodioxol-5-yl)carbonyl]oxy]aspidospermidine-3-carboxylic acid methyl ester Basic information |
Product Name: | (5α,12β,19α,20R)-2,3-Didehydro-16-methoxy-20-[[(7-methoxy-1,3-benzodioxol-5-yl)carbonyl]oxy]aspidospermidine-3-carboxylic acid methyl ester | Synonyms: | (5α,12β,19α,20R)-2,3-Didehydro-16-methoxy-20-[[(7-methoxy-1,3-benzodioxol-5-yl)carbonyl]oxy]aspidospermidine-3-carboxylic acid methyl ester;Echitoserpine;Aspidospermidine-3-carboxylic acid, 2,3-didehydro-16-methoxy-20-[[(7-methoxy-1,3-benzodioxol-5-yl)carbonyl]oxy]-, methyl ester, (5α,12R,19α,20R)- (9CI) | CAS: | 55870-82-1 | MF: | C31H34N2O8 | MW: | 562.61 | EINECS: | | Product Categories: | | Mol File: | 55870-82-1.mol | |
| (5α,12β,19α,20R)-2,3-Didehydro-16-methoxy-20-[[(7-methoxy-1,3-benzodioxol-5-yl)carbonyl]oxy]aspidospermidine-3-carboxylic acid methyl ester Chemical Properties |
| (5α,12β,19α,20R)-2,3-Didehydro-16-methoxy-20-[[(7-methoxy-1,3-benzodioxol-5-yl)carbonyl]oxy]aspidospermidine-3-carboxylic acid methyl ester Usage And Synthesis |
Description | This second alkaloid obtained from the fruit of Alstonia venenata is the 3-methoxy
derivative of the preceding base. It also forms colourless crystals from MeOH and
has a specific rotation of [α] D - 444.5° (c 0.3, CHC13). The ultraviolet spectrum
in ethanolic solution has absorption maxima at 205, 252, 301 and 325 nm with a
shoulder at 220 nm. | References | Majumder et at., Tetrahedron, 30, 2761 (1974) |
| (5α,12β,19α,20R)-2,3-Didehydro-16-methoxy-20-[[(7-methoxy-1,3-benzodioxol-5-yl)carbonyl]oxy]aspidospermidine-3-carboxylic acid methyl ester Preparation Products And Raw materials |
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