Cannabis Ruderalis

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Anhalonidine
Names
IUPAC name
(1S)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-methyl-8-isoquinolinol
Identifiers
3D model (JSmol)
ChemSpider
KEGG
UNII
  • InChI=1S/C12H17NO3/c1-7-10-8(4-5-13-7)6-9(15-2)12(16-3)11(10)14/h6-7,13-14H,4-5H2,1-3H3/t7-/m0/s1
    Key: PRNZAMQMBOFSJY-ZETCQYMHSA-N
  • InChI=1/C12H17NO3/c1-7-10-8(4-5-13-7)6-9(15-2)12(16-3)11(10)14/h6-7,13-14H,4-5H2,1-3H3/t7-/m0/s1
    Key: PRNZAMQMBOFSJY-ZETCQYMHBW
  • C[C@H]1c2c(cc(c(c2O)OC)OC)CCN1
Properties
C12H17NO3
Molar mass 223.272 g·mol−1
Melting point 160 °C (320 °F; 433 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Anhalonidine a naturally occurring alkaloid which can be isolated from certain members of the cactus family, such as Lophophora.[2] It is structurally related to mescaline.

See also[edit]

References[edit]

  1. ^ Späth, Ernst (August 1923). "Über die Anhaloniumalkaloide". Monatshefte für Chemie (in German). 43 (8): 477–484. doi:10.1007/BF01526801. S2CID 197766778.
  2. ^ Djerassi, Carl; Smith, C. R.; Marfey, S. P.; McDonald, R. N.; Lemin, A. J.; Figdor, S. K.; Estrada, H. (June 1954). "Alkaloid Studies. III.1 Isolation of Pilocereine and Anhalonidine from Four Cactus Species". Journal of the American Chemical Society. 76 (12): 3215–3217. doi:10.1021/ja01641a034.


source: https://en.wikipedia.org/wiki/Anhalonidine

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