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| (6aS)-5,6,6a,7-Tetrahydro-1,10-dimethoxy-4H-dibenzo[de,g]quinoline-2,11-diol Basic information |
Product Name: | (6aS)-5,6,6a,7-Tetrahydro-1,10-dimethoxy-4H-dibenzo[de,g]quinoline-2,11-diol | Synonyms: | (6aS)-5,6,6a,7-Tetrahydro-1,10-dimethoxy-4H-dibenzo[de,g]quinoline-2,11-diol;Lindcarpine | CAS: | 14028-95-6 | MF: | Cl8H19O4N | MW: | 0 | EINECS: | | Product Categories: | | Mol File: | 14028-95-6.mol | ![(6aS)-5,6,6a,7-Tetrahydro-1,10-dimethoxy-4H-dibenzo[de,g]quinoline-2,11-diol Structure](CAS/GIF/14028-95-6.gif) |
| (6aS)-5,6,6a,7-Tetrahydro-1,10-dimethoxy-4H-dibenzo[de,g]quinoline-2,11-diol Chemical Properties |
| (6aS)-5,6,6a,7-Tetrahydro-1,10-dimethoxy-4H-dibenzo[de,g]quinoline-2,11-diol Usage And Synthesis |
Description | The roots of Lindera pipericarpa Boer!. yield this noraporphine alkaloid which,
on recrystallization from AcOEt, forms colourless, slender needles. The base has
[α]22D + 166° (c 1.35, EtOH) and yields a hydrochloride crystallizing from
aqueous EtOH, m.p. 200°C (dec.) and the N-methyl derivative, m.p. 196°C;
[α]22D + 222° (c 0.8, MeOH). The O,N-dimethyl compound is identical with
Isocorydine (q.v.). | References | Kiang, Sim., J. Chem. Soc., C, 282 (1967) |
| (6aS)-5,6,6a,7-Tetrahydro-1,10-dimethoxy-4H-dibenzo[de,g]quinoline-2,11-diol Preparation Products And Raw materials |
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