(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol Struktur
6582-68-9
CAS-Nr.
6582-68-9
Englisch Name:
(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol
Synonyma:
Kopsanol;(22S)-Kopsan-22-ol;(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol;6H,13aH-3a,5a-Ethano-5,11-methano-1H-indolizino[8,1-cd]carbazol-14-ol, 2,3,4,5,11,12-hexahydro-, (3aR,5R,5aR,10bR,11R,13aS,14S)-
CBNumber:
CB32193497
Summenformel:
C20H24N2O
Molgewicht:
308.42
MOL-Datei:
6582-68-9.mol

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol Eigenschaften

Schmelzpunkt:
239-245°C (dec.).

Sicherheit

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

An imidazolidinocarbazole alkaloid, this base occurs in Aspidosperma duckei Hub. and also in A. macrocarpon Mart. It may be purified by recrystallization from either MeOH or CHC1 3 when it forms colourless needles. It has [α]27D + 16.7° (c 0.6, CHC13 ). The ultraviolet spectrum in ethanol solution has absorp-tion maxima at 246 and 297 mil. In 5N/HCl the absorption maxima occur at 262 and 268.5 mil with shoulders at 249 and 255 mil. The alkaloid contains one hydroxyl group and on acetylation yields the O-acetate, m.p. 202-5°C; [α]26D + 37° (c 2.97, CHCI3 ).

Einzelnachweise

Filho et al., J. Chem. Soc., C, 1260 (1966)

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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  • (22S)-Kopsan-22-ol
  • (2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol
  • Kopsanol
  • 6H,13aH-3a,5a-Ethano-5,11-methano-1H-indolizino[8,1-cd]carbazol-14-ol, 2,3,4,5,11,12-hexahydro-, (3aR,5R,5aR,10bR,11R,13aS,14S)-
  • 6582-68-9
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