salutaridine

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salutaridine Basic information
Product Name:salutaridine
Synonyms:5,6,8,14-Tetradehydro-4-hydroxy-3,6-dimethoxy-17-methylmorphinan-7-one;salutaridine;Morphinan-7-one, 5,6,8,14-tetradehydro-4-hydroxy-3,6-dimethoxy-17-methyl-
CAS:1936-18-1
MF:C19H21NO4
MW:327.37
EINECS:
Product Categories:
Mol File:1936-18-1.mol
salutaridine Structure
salutaridine Chemical Properties
Melting point 197-198°
alpha D12 +114° (c = 0.5 in methanol)
Boiling point 532.5±50.0 °C(Predicted)
density 1.33±0.1 g/cm3(Predicted)
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka9.28±0.40(Predicted)
color Pale Brown to Light Brown
Safety Information
Hazardous Substances Data1936-18-1(Hazardous Substances Data)
MSDS Information
salutaridine Usage And Synthesis
DescriptionAn alkaloid obtained from Croton salutaris, this base has been postulated as an intermediate compound in the biosynthesis of the morphine alkaloids. It yields colourless rods when crystallized from AcOEt and has [α]D + 111 ° (c 1.69, EtOH). The ultraviolet spectrum in EtOH has two absorption maxima at 240 and 277 mJl. Two methoxyl groups, a phenolic hydroxyl group and a methylimino group are present, the base furnishing an O-acetate, m.p. 171°C; [α]D + 120° (c 1.25, EtOH). More recently, it has been discovered in Croton balsamifera Jacq. and Papaver orientale.
UsesSalutaridine is one of the biosynthetic precursors of morphine (M652290), a principle alkaloid of opium.
DefinitionChEBI: Salutaridine is a morphinane alkaloid from the opium poppy, in which the 5,6,8,14-tetradehydromorphinan-7-one skeleton is substituted at position 4 by a hydroxyl group, positions 3 and 6 by methoxy groups and position N17 by a methyl group. An intermediate in the biosynthesis of narcotic analgesics such as morphine and codeine. It has a role as a metabolite and an anti-HBV agent. It is a conjugate base of a salutaridinium(1+). It derives from a hydride of a morphinan.
ReferencesBarton et al., J. Chem. Soc., 2423 (1965)
Battersby, Brown., Chem. Commun., 170 (1966)
Chambers, Haynes, Stuart., ibid, 449 (1966)
Mass spectra:
Wheeler, Kinstle, Rinehart.,J. Amer. Chem. Soc., 89,4494 (1967)
salutaridine Preparation Products And Raw materials
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