2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

The EtOH extract of Urechites karwinskii roots contains this necine base. NaBH4 reduces the ketone group to a secondary hydroxyl while Mn02 oxidizes the hydroxylmethyl group to the aldehyde.

Einzelnachweise

Del Castillo et ai., Tetrahedron Lett., 1219 (1970)

2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
Hangzhou MolCore BioPharmatech Co.,Ltd.	+86-057181025280; +8617767106207	sales@molcore.com	China	49734	58
TargetMol Chemicals Inc.	+1-781-999-5354;	support@targetmol.com	United States	39037	58
EMMX Biotechnology LLC	888-539-0666	info@emmx.com	United States	8447	60
Biosynth Biological Technology (Suzhou) Co Ltd	--	sales@biosynth.com	China	6051	58
Wuhan Zhongzhicheng Biotechnology Co., Ltd.	13628624121 13628604890	1205052329@qq.com	China	9955	58

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• 2,3-Dihydro-7-(hydroxymethyl)-1H-pyrrolizin-1-one
• 6-Hydroxymethyl-1-azabicyclo[3.3.0]octane-5,7-dien-4-one
• Loroquine
• 1H-Pyrrolizin-1-one, 2,3-dihydro-7-(hydroxymethyl)-
• 27792-82-1