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| 1-Methyl-3-oxo-2,4(1H)-cyclo-3,4-secoakuammilan-17-oic acid methyl ester Basic information |
Product Name: | 1-Methyl-3-oxo-2,4(1H)-cyclo-3,4-secoakuammilan-17-oic acid methyl ester | Synonyms: | 1-Methyl-3-oxo-2,4(1H)-cyclo-3,4-secoakuammilan-17-oic acid methyl ester;Vincoridine;13H-3,8a-Methano-1H-azepino[1',2':1,2]pyrrolo[2,3-b]indole-14-carboxylic acid, 4-ethylidene-2,3,4,5,7,8-hexahydro-13-methyl-1-oxo-, methyl ester, (3R,4E,8aR,13aS,14S)- (9CI) | CAS: | 21290-53-9 | MF: | C21H24N2O3 | MW: | 352.43 | EINECS: | | Product Categories: | | Mol File: | 21290-53-9.mol | |
| 1-Methyl-3-oxo-2,4(1H)-cyclo-3,4-secoakuammilan-17-oic acid methyl ester Chemical Properties |
Melting point | 159-160 °C | Boiling point | 513.9±50.0 °C(Predicted) | density | 1.31±0.1 g/cm3(Predicted) | pka | 3.81±0.40(Predicted) |
| 1-Methyl-3-oxo-2,4(1H)-cyclo-3,4-secoakuammilan-17-oic acid methyl ester Usage And Synthesis |
Description | A further alkaloid found in Vinca minor, this base may be crystallized from nheptane
when it yields colourless needles. It is strongly laevorotatory having
[α]D - 158° (c 0.87, CHCI3). The ultraviolet spectrum consists of two absorption
maxima at 258 and 312 mμ. | References | Mokry, Kompis., Naturwiss., 50,93 (1963) |
| 1-Methyl-3-oxo-2,4(1H)-cyclo-3,4-secoakuammilan-17-oic acid methyl ester Preparation Products And Raw materials |
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