Anhalonine

Title: Anhalonine
CAS Registry Number: 519-04-0
CAS Name: 6,7,8,9-Tetrahydro-4-methoxy-9-methyl-1,3-dioxolo[4,5-h]isoquinoline
Molecular Formula: C12H15NO3
Molecular Weight: 221.25
Percent Composition: C 65.14%, H 6.83%, N 6.33%, O 21.69%
Literature References: From mescal buttons [Lophophora williamsii (Lemaire) Coult. (Anhalonium lewinii Henn.), Cactaceae] also in Ariocarpus, in Gymnocalycium gibbosum. Synthesis of dl-form and resolution: Späth, Kesztler, Ber. 68, 1663 (1935); Brossi et al., J. Am. Chem. Soc. 93, 6248 (1971). Configuration: Battersby, Edwards, J. Chem. Soc. 1960, 1214.
Properties: Rhombic needles from petr ether, mp 86°, bp0.02 140°. [a]D25 -63.8° (methanol); -56.3° (chloroform). Very sol in alcohol, ether, chloroform, benzene, petr ether.
Melting point: mp 86°
Boiling point: bp0.02 140°
Optical Rotation: [a]D25 -63.8° (methanol); -56.3° (chloroform)
Derivative Type: Hydrochloride
Molecular Formula: C12H15NO3.HCl
Molecular Weight: 257.71
Percent Composition: C 55.93%, H 6.26%, N 5.44%, O 18.62%, Cl 13.76%
Properties: Orthorhombic prisms, dec 255°; freely sol in hot water. Aq soln is neutral.
Anidulafungin Anilazine Anileridine Aniline Aniline Mustard

Anhalonine
Anhalonine.png
Identifiers
PubChem 520752
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Anhalonine is an akaloid isolated from Lophophora williamsii.