(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one

(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one Struktur
65617-99-4
CAS-Nr.
65617-99-4
Englisch Name:
(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one
Synonyma:
Ervitsine;(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one;1,5-Methanoazonino[4,3-b]indol-7(2H)-one, 4-ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-, (1R,4E,5S)-
CBNumber:
CB92323825
Summenformel:
C19H20N2O
Molgewicht:
292.37
MOL-Datei:
65617-99-4.mol

(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one Eigenschaften

Sicherheit

(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one Chemische Eigenschaften,Einsatz,Produktion Methoden

Occurrence

An alkaloid isolated from Pandacea boiteau, this base forms colourless crystals from MeOH and is laevorotatory with a specific rotation of [α] -160° (c 1.0, CHCl3). The ultraviolet spectrum in EtOH consists of two absorption maxima at 276 and 318 nm.

(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


(1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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  • (1R,4E,5S)-4-Ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-1β,5β-methanoazonino[4,3-b]indol-7(2H)-one
  • Ervitsine
  • 1,5-Methanoazonino[4,3-b]indol-7(2H)-one, 4-ethylidene-1,3,4,5,6,8-hexahydro-2-methyl-13-methylene-, (1R,4E,5S)-
  • 65617-99-4
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