(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine

(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine Basic information
Product Name:(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine
Synonyms:(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine;Stemonine;Stemonine【C22 alkaloid】;Furo[2,3-h]pyrrolo[3,2,1-jk][1]benzazepin-10(2H)-one, 8-ethyldodecahydro-11-methyl-2-(tetrahydro-4-methyl-5-oxo-2-furanyl)-
CAS:20460-41-7
MF:C22H33NO4
MW:375.5
EINECS:
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Mol File:20460-41-7.mol
(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine Structure
(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine Chemical Properties
Melting point 151°C
Safety Information
MSDS Information
(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine Usage And Synthesis
DescriptionThis base occurs with Stemonidine (q.v.) in Stemona ovata Nakai. It is laevo_x0002_rotatory with [α]16D - 113.84° and crystallizes as colourless prisms. It gives crystalline salts such as the hydrochloride, m.p. 302°C (dec.) and is a secondary base. With methyl iodide it forms methylstemonine methiodide, m.p. 276°C (dec. ).
ReferencesSuzuki., J. Pharm. Soc., Japan, 49, 78 (1929)
Suzuki., ibid, 51,43 (1931)
Suzuki., ibid, 54, 101 (1934)
(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine Preparation Products And Raw materials
Tag:(8ξ,9ξ,10ξ,11ξ,12ξ,13ξ,14ξ)-2-(Tetrahydro-4-methyl-5-oxofuran-2-yl)stenine(20460-41-7) Related Product Information