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| (αE)-α-Ethylidene-1,2,3,3aα,4,5,6,7-octahydro-7α-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluorene-5β-acetaldehyde Basic information |
Product Name: | (αE)-α-Ethylidene-1,2,3,3aα,4,5,6,7-octahydro-7α-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluorene-5β-acetaldehyde | Synonyms: | (-)-Akagerine;(3aS,αE)-α-Ethylidene-1,2,3,3a,4,5,6,7-octahydro-7α-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluorene-5β-acetaldehyde;(αE)-α-Ethylidene-1,2,3,3aα,4,5,6,7-octahydro-7α-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluorene-5β-acetaldehyde;Akagerine;3,7a-Diazacyclohepta[jk]fluorene-5-acetaldehyde, α-ethylidene-1,2,3,3a,4,5,6,7-octahydro-7-hydroxy-3-methyl-, (αE,3aS,5R,7S)- | CAS: | 56519-07-4 | MF: | C20H24N2O2 | MW: | 324.42 | EINECS: | | Product Categories: | | Mol File: | 56519-07-4.mol | |
| (αE)-α-Ethylidene-1,2,3,3aα,4,5,6,7-octahydro-7α-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluorene-5β-acetaldehyde Chemical Properties |
Melting point | 188°C (dec.) |
| (αE)-α-Ethylidene-1,2,3,3aα,4,5,6,7-octahydro-7α-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluorene-5β-acetaldehyde Usage And Synthesis |
Description | A recently discovered alkaloid, ajmalicinine has been obtained from the root bark of
Cabucala striolata. The structure closely resembles that of the preceding base and
has been established by chemical and spectroscopic methods. | References | Bombardelli et al., Fitoterapia, 45, 183 (1974) |
| (αE)-α-Ethylidene-1,2,3,3aα,4,5,6,7-octahydro-7α-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluorene-5β-acetaldehyde Preparation Products And Raw materials |
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