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16-epi-isositsirikine

16-epi-isositsirikine Struktur
6519-27-3
CAS-Nr.
6519-27-3
Englisch Name:
16-epi-isositsirikine
Synonyma:
NSC 338932;NSC 282700;Rhazimanine;Isositsirikine;16-epi-isositsirikine;(16R)-E-Isositsirikine;(16R,19E)-19,20-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester;17,18-Secoyohimban-16-carboxylicacid,19,20-didehydro-17-hydroxy-,methylester;Methyl 2-[(12Br)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate;Indolo[2,3-a]quinolizine-2-acetic acid, 3-ethylidene-1,2,3,4,6,7,12,12b-octahydro-α-(hydroxymethyl)-, methyl ester, (αR,2R,3E,12bS)-
CBNumber:
CB51331245
Summenformel:
C21H26N2O3
Molgewicht:
354.45
MOL-Datei:
6519-27-3.mol

16-epi-isositsirikine Eigenschaften

Schmelzpunkt:
263.5℃
Siedepunkt:
558.9±50.0 °C(Predicted)
Dichte
1.26±0.1 g/cm3(Predicted)
pka
14.29±0.10(Predicted)

Sicherheit

16-epi-isositsirikine Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

An amorphous alkaloid found in Vinca rosea L., this laevorotatory base has [α]25D - 20° (CHCI3). In EtOH, the ultraviolet spectrum has absorption maxima at 224, 283 and 291 m/J.. The alkaloid forms a hemisulphate, m.p. 263.5°C and an amorphous O-acetate. The picrate is obtained in the form of brilliant yellow needles when crystallized from MeOH, m.p. 216°C.

Einzelnachweise

Kutney, Brown., Tetrahedron, 22,321 (1966)

16-epi-isositsirikine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

16-epi-isositsirikine Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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  • 16-epi-isositsirikine
  • (16R,19E)-19,20-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester
  • Isositsirikine
  • (16R)-E-Isositsirikine
  • NSC 282700
  • NSC 338932
  • Rhazimanine
  • Indolo[2,3-a]quinolizine-2-acetic acid, 3-ethylidene-1,2,3,4,6,7,12,12b-octahydro-α-(hydroxymethyl)-, methyl ester, (αR,2R,3E,12bS)-
  • 17,18-Secoyohimban-16-carboxylicacid,19,20-didehydro-17-hydroxy-,methylester
  • Methyl 2-[(12Br)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate
  • 6519-27-3
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