(3S,16S)-17α,21-Epoxy-14,15-dihydro-14α-hydroxy-12-methoxyeburnamenine-14-carboxylic acid methyl ester

(3S,16S)-17α,21-Epoxy-14,15-dihydro-14α-hydroxy-12-methoxyeburnamenine-14-carboxylic acid methyl ester Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

The root bark of Voacanga chalotiana furnishes this alkaloid which forms colourless needles when recrystallized from C6H6 . It has the following specific rotations: [α]²²_D + 30° (c 2.0, pyridine) and α]²²_D - 11 ° (c 1.0, CHCI3). The ultraviolet spectrum in MeOH has absorption maxima at 226, 270 and 292 nm.

Einzelnachweise

Bombardellietal., Tetrahedron, 30, 4141 (1974)

(3S,16S)-17α,21-Epoxy-14,15-dihydro-14α-hydroxy-12-methoxyeburnamenine-14-carboxylic acid methyl ester Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(3S,16S)-17α,21-Epoxy-14,15-dihydro-14α-hydroxy-12-methoxyeburnamenine-14-carboxylic acid methyl ester Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate

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• (3S,16S)-17α,21-Epoxy-14,15-dihydro-14α-hydroxy-12-methoxyeburnamenine-14-carboxylic acid methyl ester
• Cuanzine
• Eburnamenine-14-carboxylic acid, 17,21-epoxy-14,15-dihydro-14-hydroxy-12-methoxy-, methyl ester, (3α,14β,16α,17α)- (9CI)
• 53492-09-4