Identification | Back Directory | [Name]
tigloidine | [CAS]
495-83-0 | [Synonyms]
Tiglyssin Tigloidin tigloidine Tigloyltropine Tigloyltropeine 3α-Tigloyloxytropane 2-Methylcrotonic acid (1R,5S)-tropan-3β-yl ester | [EINECS(EC#)]
207-810-5 | [Molecular Formula]
C13H21NO2 | [MDL Number]
MFCD00867194 | [MOL File]
495-83-0.mol | [Molecular Weight]
223.314 |
Chemical Properties | Back Directory | [Boiling point ]
290.2±33.0 °C(Predicted) | [density ]
1.06±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
Oil | [pka]
10.03±0.40(Predicted) | [color ]
Light yellow to yellow |
Hazard Information | Back Directory | [Description]
A tropine alkaloid isolated from Duboisia rnyoporoides, this base is a colourless
syrup which yields crystalline salts. The hydrobromide forms colourless, tabular
crystals m.p. 234-5°C and is optically inactive; the aurichloride crystallizes as
yellow plates, m.p. 213.5- 2140 C; the picrate as yellow rectangular plates, m.p.
239°C and the methiodide as square plates, m.p. 244-5°C. The alkaloid is
unsaturated and the hydro bromide, on hydrogenation, furnishes dihydrotigloidine,
giving a picrate, m.p. l34-5°C. When treated with bromine in CHC13 it forms
dibromodihydrotigloidine, m.p. 187°C (dec.). The free base may be hydrolyzed
by boiling with H20 when it furnishes pseudotropine and tiglic acid. The base is
therefore the tiglyl ester of pseudotropine. By comparison, tiglyltropine gives a
hydrobromide with m.p. 207°C and a picrate, m.p. 200°C. | [storage]
Store at -20°C | [References]
Barger, Martin, Mitchel1.,J. Chern. Soc., 1820 (1937) |
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