(16α,19E)-1-Acetyl-19,20-didehydrocuran-17-ol Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

This alkaloid has been isolated from Strychnos holstii var. reticulata f. condensata and may be purified by recrystallization from AcOEt or heptane when it yields clusters of colourless needles. It is dextrorotatory with [α]_D + 23° (c 0.7, MeOH) and gives an ultraviolet spectrum which exhibits a single absorption maximum at 254.4 mIJ.. It is only sparingly soluble in heptane or Et20, more so in C6H6 and freely soluble in MeOH, EtOH, Me2CO or CHC13. The alkaloid has been synthesized via the lactam produced from strychnine or the WielandGumlich aldehyde.

Einzelnachweise

Bosley.,J. Pharrn. Belg., 6,150,243 (1951)
Structure:
Bisset., Chern. Ind., 1036 (1965)
Synthesis:
Wenkert, Sklar.,J. Org. Chern., 31,2689 (1966)
Hymon, Schmid., Helv. Chirn. Acta., 49,2067 (1966)

(16α,19E)-1-Acetyl-19,20-didehydrocuran-17-ol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(16α,19E)-1-Acetyl-19,20-didehydrocuran-17-ol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
TargetMol Chemicals Inc.		support@targetmol.com	United States	38631	58
Shanghai Youji Materials Co., Ltd	13052376889 13681663468	2851911691@qq.com	China	824	58

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• (16α,19E)-1-Acetyl-19,20-didehydrocuran-17-ol
• Retuline
• Curan-17-ol, 1-acetyl-19,20-didehydro-, (16α,19E)-
• (16α,19E)-1-Acetyl-19,20-didehydrocuran-17-ol
• 2616-16-2