Exploring Eugenol. To explore a different substance…

Names:
Eugenol · 4-Hydroxy-3-methoxyphenylprop-2-ene
IUPAC name:
2-Methoxy-4-(prop-2-en-1-yl)phenol
ID: 1121 · Formula: C10H12O2 · Molecular weight: 164.201
InChI: InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3,5-7,11H,1,4H2,2H3

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

Shulgin, AT. Concerning the pharmacology of nutmeg. Mind, 1 Jan 1963, 1, 299–302. 578 kB.

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.

Methyleugenol
5-Methoxyeugenol
1122
Isoeugenol
3-MT
N-Me-GEA
MM-GEA
MHA
β-Me-GEA
Normetanephrine
Metanephrine
β-HO-N-iPr-GEA
GEA-βk
N-Me-GEA-βk
MHAOH
MHMA
MHMAOH
MHEA
MHMC
MH-α-Et-PEA
N-Me-α-Et-GEA
bk-MBDB-M1
bk-MDEA-M1
1122
Isoeugenol
Chavibetol
1132
1133
4-MeOP2P
1147
1149
1150
1153
Methyleugenol
5-Methoxyeugenol
1122
Isoeugenol
3-MT
N-Me-GEA
MM-GEA
MHA
β-Me-GEA
Normetanephrine
Metanephrine
β-HO-N-iPr-GEA
GEA-βk
N-Me-GEA-βk
MHAOH
MHMA
MHMAOH
MHEA
MHMC
MH-α-Et-PEA
N-Me-α-Et-GEA
bk-MBDB-M1
bk-MDEA-M1
1122
Isoeugenol
Chavibetol
1132
1133
4-MeOP2P
1147
1149
1150
1153
24 July 2017 · Creative Commons BY-NC-SA ·