Exploring Isoeugenol. To explore a different substance…

Names:
Isoeugenol
trans-4-Hydroxy-3-methoxyphenylprop-1-ene
IUPAC name:
2-Methoxy-4-[(1E)-prop-1-en-1-yl]phenol
1123 · C10H12O2 · 164.201
Essential oil
InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3-7,11H,1-2H3/b4-3+
BJIOGJUNALELMI-ONEGZZNKSA-N This stereoisomer Any stereoisomer

Shulgin, AT. Composition of the myristicin fraction from oil of nutmeg. Nature, 1 Jan 1963, 197, 379. 107 kB. https://doi.org/10.1038/197379a0 Rhodium.

Shulgin, AT; Sargent, T; Naranjo, C. The chemistry and psychopharmacology of nutmeg and of several related phenylisopropylamines. In Ethnopharmacologic Search for Psychoactive Drugs; Efron, DH; Holmstedt, B; Kline, NS, Eds., U.S. Department of Health and Human Services, National Institute of Health, U.S. Government Printing Office, Washington, DC, 28 Jan 1967; pp 202–215. 951 kB.

Weil, AT. The use of nutmeg as a psychotropic agent. Bull. Narc., United Nations Office on Drugs and Crime, 1 Jan 1966.

Shulgin, AT. The narcotic pepper—The chemistry and pharmacology of Piper methysticum and related species. Bull. Narc., 1 Jan 1973, 25 (2), 61–77. 325 kB. #XII UNODC.

Eugenol
1122
Chavibetol
1132
1133
4-MeOP2P
1147
1149
1150
1153
4-Propoxybenzaldehyde
21 August 2018 · Creative Commons BY-NC-SA ·