Anhalidine

Anhalidine
Names

IUPAC name 6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydro-8-isoquinolinol
Identifiers
CAS Number	2245-94-5
3D model (JSmol)	Interactive image
ChemSpider	2033430
PubChem CID	2752318
InChI InChI=1S/C12H17NO3/c1-13-5-4-8-6-10(15-2)12(16-3)11(14)9(8)7-13/h6,14H,4-5,7H2,1-3H3 Key: DTXOXOHMRGAFDX-UHFFFAOYSA-N InChI=1/C12H17NO3/c1-13-5-4-8-6-10(15-2)12(16-3)11(14)9(8)7-13/h6,14H,4-5,7H2,1-3H3 Key: DTXOXOHMRGAFDX-UHFFFAOYAS
SMILES OC1=C(C(OC)=CC2=C1CN(C)CC2)OC
Properties
Chemical formula	C₁₂H₁₇NO₃
Molar mass	223.268
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Anhalidine is a naturally occurring tetrahydroisoquinoline based alkaloid which can be isolated from Lophophora williamsii;^[1] it has also been detected other cactii^[2] and several species of Acacia.^[3]^[4] It is part of a family of compounds that are structurally related to Mescaline.

References

↑ Lundström, Jan; Agurell, Stig (1967). "Thin-layer chromatography of the peyote alkaloids". Journal of Chromatography A. 30: 271–272. ISSN 0021-9673. doi:10.1016/S0021-9673(00)84157-6.
↑ Roush, Robin A.; Cooks, R. Graham.; Sweetana, Stephanie A.; McLaughlin, Jerry L. (1985). "Search for new alkaloids in Pachycereus weberi by tandem mass spectrometry". Analytical Chemistry. 57 (1): 109–114. ISSN 0003-2700. doi:10.1021/ac00279a030.
↑ Clement, Beverly A.; Goff, Christina M.; Forbes, T. David A. (1997). "Toxic amines and alkaloids from Acacia berlandieri". Phytochemistry. 46 (2): 249–254. ISSN 0031-9422. doi:10.1016/S0031-9422(97)00240-9.
↑ Clement, Beverly A; Goff, Christina M; Forbes, T.David A (1998). "Toxic amines and alkaloids from acacia rigidula". Phytochemistry. 49 (5): 1377–1380. ISSN 0031-9422. doi:10.1016/S0031-9422(97)01022-4.

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