| Identification | Back Directory | [Name]
sabadine | [CAS]
124-80-1 | [Synonyms]
sabadine
Sabatine
Einecs 204-714-5
Cevane-3β,4α,12,14,16β,17,20-heptol 3-acetate
3β-Acetyloxycevane-4α,12α,14α,16β,17α,20β-hexol
3β-Acetyloxycevane-4α,12α,14α,16β,17α,20β,-hexaol
Cevane-3,4,12,14,16,17,20-heptol, 3-acetate, (3β,4α,16β)-
Cevane-3,4,12,14,16,17,20-heptol, 3-acetate, (3beta,4alpha,16-beta)- | [EINECS(EC#)]
204-714-5 | [Molecular Formula]
C29H47NO8 | [MOL File]
124-80-1.mol | [Molecular Weight]
537.69 |
| Chemical Properties | Back Directory | [Melting point ]
256-258° (dec) | [alpha ]
D25 -11° (c = 1.93 in alc) | [Boiling point ]
614.28°C (rough estimate) | [density ]
1.1622 (rough estimate) | [refractive index ]
1.6290 (estimate) | [pka]
13.19±0.70(Predicted) | [EPA Substance Registry System]
Cevane-3,4,12,14,16,17,20-heptol, 3-acetate, (3.beta.,4.alpha.,16-.beta.)- (124-80-1) |
| Hazard Information | Back Directory | [Description]
This alkaloid was isolated by Merck from the seeds of Schoenocaulon officinale. A. Gray. It crystallizes from Et20 in colourless needles and forms crystalline salts, e.g. the hydrochloride as the dihydrate, m.p. 282-4°C (dry, dec.); nitrate which is sparingly soluble in H20 and the aurichloride which forms goldenyellow needles. | [References]
Merck., Chern. Soc. Abstr., 60,844 (1891) |
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