1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone

1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone Struktur
6384-73-2
CAS-Nr.
6384-73-2
Englisch Name:
1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone
Synonyma:
Samandaridine;1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone;2,5-Epoxyfuro[3'',2'':3',4']cyclopenta[1',2':5,6]naphth[1,2-d]azepin-9(1H)-one, octadecahydro-5a,7a-dimethyl-, (2S,5R,5aS,5bS,7aS,7bR,10aS,11aS,11bS,13aR)-
CBNumber:
CB52228272
Summenformel:
C21H31NO3
Molgewicht:
345.48
MOL-Datei:
6384-73-2.mol

1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone Eigenschaften

Schmelzpunkt:
287-8°C
Siedepunkt:
498.9±45.0 °C(Predicted)
Dichte
1.153±0.06 g/cm3(Predicted)
pka
8.69±0.60(Predicted)

Sicherheit

1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

A hex acyclic alkaloid present in the skin secretions of various species of Salamandra (salamanders), the base yields a crystalline hydrochloride, m.p. 343°C; [α]24578 + 14.1° and a hydrobromide which crystallizes from MeOH with solvent of crystallization, m.p. 346°C. The structure has been determined from the infrared, NMR and mass spectra.

Einzelnachweise

Schopf, Koch., Annalen, 552,41 (1942)
Habermehl., Chem. Ber., 96, 143,840 (1963)

1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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  • 1α,4α-Epoxy-16β-hydroxy-3-aza-A-homo-5β-pregnan-21-oic acid γ-lactone
  • Samandaridine
  • 2,5-Epoxyfuro[3'',2'':3',4']cyclopenta[1',2':5,6]naphth[1,2-d]azepin-9(1H)-one, octadecahydro-5a,7a-dimethyl-, (2S,5R,5aS,5bS,7aS,7bR,10aS,11aS,11bS,13aR)-
  • 6384-73-2
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