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24240-05-9

24240-05-9 Structure

24240-05-9 Structure
IdentificationBack Directory
[Name]

Pseudo protopine
[CAS]

24240-05-9
[Synonyms]

Pseudo protopine
Pseudoprotopine >=95% (LC/MS-ELSD)
Bis[1,3]benzodioxolo[5,6-c:5',6'-g]azecin-14(6H)-one, 5,7,8,15-tetrahydro-6-methyl-
[Molecular Formula]

C20H19NO5
[MDL Number]

MFCD24849361
[MOL File]

24240-05-9.mol
[Molecular Weight]

353.37
Chemical PropertiesBack Directory
[Melting point ]

200-10C
[Boiling point ]

551.6±49.0 °C(Predicted)
[density ]

1.323±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[form ]

solid
[pka]

7.88±0.20(Predicted)
[Major Application]

metabolomics
vitamins, nutraceuticals, and natural products
[InChI]

1S/C20H19NO5/c1-21-3-2-12-5-17-20(26-11-23-17)8-15(12)16(22)4-13-6-18-19(25-10-24-18)7-14(13)9-21/h5-8H,2-4,9-11H2,1H3
[InChIKey]

ZAALQOFZFANFTF-UHFFFAOYSA-N
[SMILES]

N1(CCc2c(cc5c(c2)OCO5)C(=O)Cc3c(cc4c(c3)OCO4)C1)C
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

50
[Safety Statements ]

61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Aquatic Acute 1
Aquatic Chronic 1
Hazard InformationBack Directory
[Description]

An alkaloid obtained from Zanthoxylum conspersipunctatum Merr. & Perry, the base yields colourless crystals from MeOH and is optically inactive. The above structure has recently been confirmed by synthesis of the alkaloid.
[General Description]

Natural product derived from plant source.
[References]

Johns et at., Austral. J. Chern., 22, 2233 (1969)
Synthesis: Sotelo, Giacopello., Austral. J. Chern., 25,385 (1972)
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