(17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate

(17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

An alkaloid from Rauwolfia vomitora, the base yields colourless crystals from MeOH and has [α]_D - 173.4° ± 1° (c 1.0, CHCl 3). The hydrochloride has m.p. 223° C (dec.). Acid hydrolysis of the base furnishes tetraphyllicine and gallic acid trimethyl ether.

Einzelnachweise

Haack, Popelak, Springler., Naturwiss., 42,627 (1955)
Poisson, Goutarel, Janot., Compt. rend., 241, 1840 (1955)
Bartlett et al., J. Amer. Chem. Soc., 84,622 (1962)

(17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
TargetMol Chemicals Inc.	+1-781-999-5354	support@targetmol.com	United States	19973	58
Wuhan ChemFaces Biochemical Co., Ltd.	18607101326 15172504745	aileen@chemfaces.com	China	7059	55
EMMX Biotechnology LLC	888-539-0666	info@emmx.com	United States	8449	60
Sichuan BioCrick Biotech Co., Ltd	28-85433893	info@biocrick.com	CHINA	4988	58

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• (17R,19E)-19,20-Didehydroajmalan-17-ol 3,4,5-trimethoxybenzoate
• Rauvomitine
• Rauvomitin
• Ajmalan-17-ol, 19,20-didehydro-, 17-(3,4,5-trimethoxybenzoate), (17R,19E)-
• 466-57-9