Log in | Join Free | china | japan | germany

(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one

Request For Quotation
(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one Basic information
Product Name:(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one
Synonyms:(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one;Oxotuberostemonine;2H-Furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one, 5-ethyl-3,3a,4,5,6,7,8,9,11,12-decahydro-4-hydroxy-3-methyl-11-[(2S,4S)-tetrahydro-4-methyl-5-oxo-2-furanyl]-, (3S,3aS,4S,5R,11S,12aS)-;(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one
CAS:20675-62-1
MF:C22H31NO5
MW:389.49
EINECS:
Product Categories:
Mol File:20675-62-1.mol
(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one Structure
(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one Chemical Properties
Melting point 217（222°）
Safety Information
MSDS Information
(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one Usage And Synthesis
DescriptionThis minor alkaloid obtained from several species of Sternona, particularly the roots of S. tuberosa, forms flat, shiny needles when crystallized from MeOH. The ultraviolet spectrum has a single absorption maximum at 243 mJ.1. The base remains in the mother liquor following the removal of Tuberostemonine (q.v.) and is soluble in most organic solvents although only sparingly so in Et20. It is insoluble in petroleum ether.
ReferencesKondo, Satomi, Odera., Ann. Rep. ITSUU Lab. (Tokyo), 5, 99 (1954)
Pailer, Belohlov., Monatsh., 85, 1055 (1954)
Edwards, Feniak, Honda., Can. J. Chern., 40,455 (1962)
(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one Preparation Products And Raw materials
Tag:(3S,12aS)-5α-Ethyl-3,3aα,4,5,6,7,8,9,11,12-decahydro-4β-hydroxy-3-methyl-11α-[(2S,4S)-tetrahydro-4-methyl-5-oxofuran-2-yl]-2H-furo[3,2-i]pyrrolo[3,2,1-jk][1]benzazepin-2-one(20675-62-1) Related Product Information