Weight | 208.257 g/mol |
---|---|
Formula | C12H16O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 5 |
Elemicin (487-11-6)
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LabBot
- Genotoxicity of the alkenylbenzenes and -asarone, myristicin and elemicin as determined by the UDS assay in cultured rat hepatocytes (Food and Chemical Toxicology, 1994)
- (E)-Methylisoeugenol and elemicin: antibacterial components of Daucus carota L. essential oil against Campylobacter jejuni. (Journal of Agricultural and Food Chemistry, 2007)
- Abuse of nutmeg (Myristica fragrans Houtt.): studies on the metabolism and the toxicologic detection of its ingredients elemicin, myristicin, and safrole in rat and human urine using gas chromatography/mass spectrometry. (Therapeutic Drug Monitoring, 2006)
- Metabolism of alkenebenzene derivatives in the rat III. Elemicin and isoelemicin (Xenobiotica, 1980)
- Physiologically based kinetic models for the alkenylbenzene elemicin in rat and human and possible implications for risk assessment. (Chemical Research in Toxicology, 2012)
- Constituents of aromatic plants: elemicin. (Fitoterapia, 2004)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC(=CC(=C1OC)OC)CC=C
-
InChIKeyBPLQKQKXWHCZSS-UHFFFAOYSA-N
- Pubchem - Elemicin
- Wikipedia - 3,4,5-trimethoxyallyl benzene
Elemicin is a phenylpropene, a natural organic compound, and is a constituent of several plant species' essential oils.
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Synthesis
Reactant
+
Methyl hydroperoxide
(Dakin oxidation)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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