|
|
| | 1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan Basic information |
| Product Name: | 1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan | | Synonyms: | Schelhammericine;1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan;2H,4H-[1,3]Dioxolo[4,5-h]indolo[7a,1-a][2]benzazepine, 1,5,6,12,13,14-hexahydro-13-methoxy-, (11bS,13R)- | | CAS: | 21030-78-4 | | MF: | C19H23NO3 | | MW: | 313.39 | | EINECS: | | | Product Categories: | | | Mol File: | 21030-78-4.mol | ![1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan Structure](CAS/20180808/GIF/21030-78-4.gif) |
| | 1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan Chemical Properties |
| | 1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan Usage And Synthesis |
| Description | This alkaloid, isolated from Schelhammera pedunculata F. Muell, has the homoerythrina structure given above which is based upon chemical and spectroscopic evidence and comparison with the two following bases. It is dextrorotatory with [α]D + 122° (CHCI3). A methoxyl and a methylenedioxy group are present as su bstituents. | | References | Johns et al., Chem. Commun., 1102 (1968) |
| | 1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan Preparation Products And Raw materials |
|