[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside

[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside Struktur
23544-46-9
CAS-Nr.
23544-46-9
Englisch Name:
[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside
Synonyma:
Ipalbine;4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside;[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside;β-D-Glucopyranoside, 4-[(8aS)-1,2,3,5,8,8a-hexahydro-7-methyl-6-indolizinyl]phenyl
CBNumber:
CB02345493
Summenformel:
C21H29NO6
Molgewicht:
391.46
MOL-Datei:
23544-46-9.mol

[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside Eigenschaften

Schmelzpunkt:
118 °C
Siedepunkt:
615.6±55.0 °C(Predicted)
Dichte
1.38±0.1 g/cm3(Predicted)
pka
12.83±0.70(Predicted)

Sicherheit

[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

This alkaloid, which is the O-~-D-glucoside of ipalbidine, also occurs in Ipomoea alba L. It is dextrorotatory with [α]23D + 32.5° (c 0.03, EtOH). The structure has been confirmed by the total synthesis from 2-methoxypyrroline and the methyl ester of acetylacetic acid.

Einzelnachweise

Gourley et al., Chem. Commun., 709 (1969) Total synthesis: Wick, Bartlett, Dolphin., Helv. Chim. Acta., 54, 513 (1971)

[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


[4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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  • [4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside
  • Ipalbine
  • β-D-Glucopyranoside, 4-[(8aS)-1,2,3,5,8,8a-hexahydro-7-methyl-6-indolizinyl]phenyl
  • 4-(1,2,3,5,8,8a-Hexahydro-7-methylindolizin-6-yl)phenyl]β-D-glucopyranoside
  • 23544-46-9
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