Exploring Elemicin. To explore a different substance…

Names:
Elemicin
3,4,5-Trimethoxyphenylprop-2-ene
IUPAC name:
1,2,3-Trimethoxy-5-(prop-2-en-1-yl)benzene
ID: 1041 · Formula: C12H16O3 · Molecular weight: 208.254
Tags: Essential oil
InChI: InChI=1S/C12H16O3/c1-5-6-9-7-10(13-2)12(15-4)11(8-9)14-3/h5,7-8H,1,6H2,2-4H3
InChI Key: BPLQKQKXWHCZSS-UHFFFAOYSA-NThis stereoisomerAny stereoisomer

Shulgin, AT. Synthesis of the trimethoxyphenylpropenes. Can. J. Chem., 1 Jan 1965, 43 (12), 3437–3440. 295 kB. https://doi.org/10.1139/v65-478

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. Possible implication of myristicin as a psychotropic substance. Nature, 1 Jan 1966, 210, 380–384. 707 kB. https://doi.org/10.1038/210380a0

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

Shulgin, AT. The separation and identification of the components of the aromatic ether fraction of essential oils by gas-liquid chromatography. J. Chromatogr. A, 1 Jan 1967, 30, 54–61. 769 kB. https://doi.org/10.1016/S0021-9673(00)84112-6

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.

cis-Isoelemicin
Isoelemicin
γ-Asarone
β-Asarone
α-Asarone
12224
2C-E aldehyde
24 May 2018 · Creative Commons BY-NC-SA ·