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| | 13,14-Dihydro-6-hydroxy-12-methoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine Basic information |
| Product Name: | 13,14-Dihydro-6-hydroxy-12-methoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine | | Synonyms: | 13,14-Dihydro-6-hydroxy-12-methoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine;Methoxychelidonine | | CAS: | | | MF: | C20H15NO6 | | MW: | 365.3362 | | EINECS: | | | Product Categories: | | | Mol File: | Mol File | ![13,14-Dihydro-6-hydroxy-12-methoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine Structure](CAS/20200119/GIF/CB32181081.gif) |
| | 13,14-Dihydro-6-hydroxy-12-methoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine Chemical Properties |
| | 13,14-Dihydro-6-hydroxy-12-methoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine Usage And Synthesis |
| Description | This alkaloid has been obtained by Gadamer and Winterfeld during a systematic
examination of the residues remaining after the isolation of chelidonine from
Chelidonum majus L. The base forms colourless prisms on crystallization from
EtOH and has [α]D + 115.8°. It furnishes a crystalline hydrochloride and an
aurichloride, m.p. 237-8°C. The O-acetate is amorphous, m.p. 147°C; [α]D +
55.5°. One methoxyl group, two methylenedioxy groups, one hydroxyl group
and a methylimino group are present in the molecule. | | References | Gadamer, Winterfeld., Arch. Pharm., 257,298 (1919)
Garlamer, Winterfeld., ibid, 258, 148 (1920)
Gadamer, Winterfeld., ibid, 262,249 (1924)
Bruchhausen, Bersch., Ber., 63,2520 (1930)
Bruchhausen, Bersch., ibid, 64,370 (1931) |
| | 13,14-Dihydro-6-hydroxy-12-methoxy[1,3]benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridine Preparation Products And Raw materials |
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