| Identification | Back 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 Properties | Back 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 Data | Back 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 Information | Back 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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Sigma-Aldrich
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Energy Chemical
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Merck KGaA
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