(5R,10S)-10,11-Dihydro-3,7,8-trimethoxy-12-methyl-10,5-(iminomethano)-5H-dibenzo[a,d]cyclohepten-2-ol Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

This alkaloid has been isolated from the roots of Thalictrum dasycarpum Fisch. et al. It crystallizes as colourless rods from Et20 or needles from EtOH. It has a specific rotation of[α]²⁵_D - 210° (c 0.21, CHCI3) and gives an ultraviolet spectrum in EtOH with a single absorption maximum at 289 nm. The methyl ether forms needles from Et20-EtOH with m.p. 91-2°C. The structure has been proved by total synthesis of the base.

Einzelnachweise

Kupchan, Yoshitaka,J. Org. Chem., 34,1062 (1969)

(5R,10S)-10,11-Dihydro-3,7,8-trimethoxy-12-methyl-10,5-(iminomethano)-5H-dibenzo[a,d]cyclohepten-2-ol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(5R,10S)-10,11-Dihydro-3,7,8-trimethoxy-12-methyl-10,5-(iminomethano)-5H-dibenzo[a,d]cyclohepten-2-ol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate

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• (5R,10S)-10,11-Dihydro-3,7,8-trimethoxy-12-methyl-10,5-(iminomethano)-5H-dibenzo[a,d]cyclohepten-2-ol
• Thalisopavine
• 10,5-(Iminomethano)-5H-dibenzo[a,d]cyclohepten-2-ol, 10,11-dihydro-3,7,8-trimethoxy-12-methyl-, (5R)- (9CI)
• 18927-72-5