6-Methoxy-1,3-dioxolo[4,5-h]furo[2,3-b]quinoline Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Terasaka has isolated this furoquinoline alkaloid from the roots of Orixa japonica and Obata has found that it also occurs in the fruit along with skim_x0002_mianine (q.v.). The alkaloid is optically inactive and is converted by Mel at 100°C into isokokusagine, m.p. 247°C. The aurichloride has m.p. 171°C and the picrate, m.p. 178°C (157°C according to Obata). The structure has been established by synthesis as 7: 8-methylenedioxydictamnine.

Einzelnachweise

Terasaka.,J. Pharm. Soc. Japan, 51,99 (1931)
Obata., ibid, 59,136 (1939)
Structure:
Terasaka et at., Chem. Pharm. Bull. (Tokyo), 2, 159 (1954)

6-Methoxy-1,3-dioxolo[4,5-h]furo[2,3-b]quinoline Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

6-Methoxy-1,3-dioxolo[4,5-h]furo[2,3-b]quinoline Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate

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• 6-Methoxy-1,3-dioxolo[4,5-h]furo[2,3-b]quinoline
• 1,3-Dioxolo[4,5-h]furo[2,3-b]quinoline, 6-methoxy-
• Kokusagine
• 482-32-6