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| | 16-[(1S)-2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-17-norcorynan Basic information |
| Product Name: | 16-[(1S)-2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-17-norcorynan | | Synonyms: | 16-[(1S)-2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-17-norcorynan;Ochrolifuanine B;Indolo[2,3-a]quinolizine, 3-ethyl-1,2,3,4,6,7,12,12b-octahydro-2-[[(1S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl]methyl]-, (2S,3R,12bS)- (9CI) | | CAS: | 35471-11-5 | | MF: | C29H34N4 | | MW: | 438.61 | | EINECS: | | | Product Categories: | | | Mol File: | 35471-11-5.mol | ![16-[(1S)-2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-17-norcorynan Structure](CAS/20210305/GIF/35471-11-5.gif) |
| | 16-[(1S)-2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-17-norcorynan Chemical Properties |
| Boiling point | 662.4±50.0 °C(Predicted) | | density | 1.26±0.1 g/cm3(Predicted) | | pka | 17.74±0.40(Predicted) |
| | 16-[(1S)-2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-17-norcorynan Usage And Synthesis |
| Description | This stereoisomer of ochrolifuanine A also occurs in the leaves of Ochrosia
lifuana Guill. It possesses only a small specific rotation of [α]20D +
0.1 ° (c 1.0,
EtOH) which appears to be real and not due to experimental error. | | References | Peube-Locou etal., Cornpt. Rend., 273C, 905 (1971) |
| | 16-[(1S)-2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl]-17-norcorynan Preparation Products And Raw materials |
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