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| | isotalatizidine Basic information |
| Product Name: | isotalatizidine | | Synonyms: | isotalatizidine;1-Isotalatisidine;20-Ethyl-16β-methoxy-4-(methoxymethyl)aconitane-1α,8,14α-triol;iso-Talatisidine;Aconitane-1,8,14-triol, 20-ethyl-16-methoxy-4-(methoxymethyl)-, (1α,14α,16β)-;Isotalatisidine | | CAS: | 7633-68-3 | | MF: | C23H37NO5 | | MW: | 407.54 | | EINECS: | | | Product Categories: | | | Mol File: | 7633-68-3.mol |  |
| | isotalatizidine Chemical Properties |
| Melting point | 140-2°C | | Boiling point | 560.6±50.0 °C(Predicted) | | density | 1.31±0.1 g/cm3(Predicted) | | pka | 13.70±0.70(Predicted) |
| | isotalatizidine Usage And Synthesis |
| Description | This atisine alkaloid has been isolated from Aconitum talassicum and Delphinium
denudatum thereby providing a link between the bases of these two genera. From
moist solvents, the alkaloid forms a crystalline monohydrate, m.p. 116-7°C.
The methiodide has m.p. 200°C and the oxalate, m.p. 185-6°C. Three hydroxylgroups are present which may be acetylated. The 10-acetate is identical with
Condelphine (q.v.); the 1: 10-diacetate has m.p. 112-7°C and the triacetate,
m.p. 130-4°C. | | References | Rabinovitch, Konovalova., Bull. Soc. Chirn. Fr., 7,95 (1940)
Kuzovkov, Platonova., J. Gen. Chern., USSR, 1286 (1961)
Pelletier, Keith, Parthsarathy., Tetrahedron Lett., 4217 (1966)
Pelletier, Keith, Parthsarathy., J. Arner. Chern. Soc., 89,4146 (1967) |
| | isotalatizidine Preparation Products And Raw materials |
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