Anhalinine
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Names | |
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Preferred IUPAC name
6,7,8-Trimethoxy-1,2,3,4-tetrahydroisoquinoline | |
Identifiers | |
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Properties | |
C12H17NO3 | |
Molar mass | 223.272 g·mol−1 |
Melting point | 60–61 °C (140–142 °F; 333–334 K)[1] |
Boiling point | 144–145 °C (291–293 °F; 417–418 K)[1] at 0.1 Torr |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Anhalinine is a naturally occurring alkaloid[2] which can be isolated from Lophophora williamsii. It is structurally related to mescaline.
See also[]
References[]
- ^ a b Taylor, E. P. (1952). "236. Synthetic neuromuscular blocking agents. Part III. Miscellaneous quaternary ammonium salts". Journal of the Chemical Society (Resumed): 1309. doi:10.1039/jr9520001309.
- ^ Ghansah, E.; Kopsombut, P.; Maleque, M.A.; Brossi, A. (February 1993). "Effects of mescaline and some of its analogs on cholinergic neuromuscular transmission". Neuropharmacology. 32 (2): 169–174. doi:10.1016/0028-3908(93)90097-M.
Categories:
- Lophophora
- Isoquinoline alkaloids
- Norsalsolinol ethers
- Pyrogallol ethers
- Alkaloid stubs