|
| (4bα,7E,8aβ,10aα)-Tetradecahydro-9β-hydroxy-1α,4aβ,8α-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-1β-phenanthrenecarboxylic acid methyl ester Basic information |
Product Name: | (4bα,7E,8aβ,10aα)-Tetradecahydro-9β-hydroxy-1α,4aβ,8α-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-1β-phenanthrenecarboxylic acid methyl ester | Synonyms: | (4bα,7E,8aβ,10aα)-Tetradecahydro-9β-hydroxy-1α,4aβ,8α-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-1β-phenanthrenecarboxylic acid methyl ester;Norerythrosuamine | CAS: | 36150-74-0 | MF: | C24H37NO6 | MW: | 435.55368 | EINECS: | | Product Categories: | | Mol File: | 36150-74-0.mol | |
| (4bα,7E,8aβ,10aα)-Tetradecahydro-9β-hydroxy-1α,4aβ,8α-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-1β-phenanthrenecarboxylic acid methyl ester Chemical Properties |
| (4bα,7E,8aβ,10aα)-Tetradecahydro-9β-hydroxy-1α,4aβ,8α-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-1β-phenanthrenecarboxylic acid methyl ester Usage And Synthesis |
Description | An amorphous minor alkaloid obtained from Erythrophleurn guineense, this
base has [α] 20
D- 71.9° (c 0.44, EtOH). The structure has been determined from
the infrared, NMR and mass spectra. Oxidation with chromic acid yields the
dehydro-compound (q.v.) which also occurs naturally. | References | Friedrich-Fiechtl, Spiteller., Chern. Ber., 104, 3535 (1971) |
| (4bα,7E,8aβ,10aα)-Tetradecahydro-9β-hydroxy-1α,4aβ,8α-trimethyl-7-[2-[2-(methylamino)ethoxy]-2-oxoethylidene]-10-oxo-1β-phenanthrenecarboxylic acid methyl ester Preparation Products And Raw materials |
|