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(5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol Suppliers list
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| | (5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol Basic information |
| Product Name: | (5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol | | Synonyms: | (5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol;Capuronine | | CAS: | | | MF: | C19H26N20 | | MW: | 0 | | EINECS: | | | Product Categories: | | | Mol File: | Mol File | ![(5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol Structure]() |
| | (5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol Chemical Properties |
| | (5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol Usage And Synthesis |
| Description | A further alkaloid obtained from the leaves and stem bark of Capuronetta eiegans,
the strucutre of this base has also been established by chemical and spectroscopic
methods. It forms colourless crystals when purified by recrystallization from
MeOH and has a specific rotation of [α]D20 + 70° (c 1.0, CHCI3). The ultraviolet
spectrum in EtOH has absorption maxima at 229,286 and 293 nm. The base may
be characterized as the O-acetate which crystallizes as colourless needles from
MeOH with m.p. 135°C. The structure given shows that capuronine is an isomer
of velbanamine. | | References | Chardon-Loriaux, Husson, Tetrahedron Lett., 1845 (1975) |
| | (5S,6S,7R)-5-Ethyl-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indol-6-ol Preparation Products And Raw materials |
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