CasNo: 93-16-3
Molecular Formula: C11H14O2
Preparation |
By methylation of isoeugenol with methyl sulfate in alkaline solution |
Toxicity evaluation |
The acute oral LD50 in rats was reported as 1.5 g/kg (Jenner, Hagan, Taylor, Cook & Fitzhugh, 1964) and as 2.5 g/kg (2.03-3.08 g/kg) (Keating, 1972). The ip LD50 in mice was reported as 0.5 g/kg for the eis- isomer and as 0.35 g/kg for the trans- isomer (Caujolle & Meynier, 1960). The acute dermal LD50 in rabbits exceeded 5 g/kg (Keating, 1972) |
General Description |
Methyl isoeugenol is one of the main components found in the essential oil extracted from Acorus calamus, bark of Croton malambo and rhizomes of Zingiber zerumbet, Hedychium coronarium and Etlingera cevuga. |
InChI:InChI=1/C11H14O2/c1-4-5-9-6-7-10(12-2)11(8-9)13-3/h4-8H,1-3H3/b5-4-
Regio- and enantioselective hydroarylami...
Dimethyl sulfide, a major byproduct of t...
Background: A new series of O-benzyloxim...
An isoeugenol 4-O-methyltransferase (IeO...
1,2-Dimethoxy-4-<3-fluoro-3-(phenylsulfonyl)-2-propenyl>benzene
1,2-dimethoxy-4-(2-propenyl)benzene
Z-1,2-Dimethoxy-4-(3-fluoro-2-propenyl)benzene
(E)-1,2-Dimethoxy-4-(3-fluoro-2-propenyl)benzene
Methylisoeugenol
Conditions | Yield |
---|---|
With
disodium hydrogenphosphate; sodium amalgam;
In
tetrahydrofuran; methanol;
at 25 ℃;
for 0.333333h;
Product distribution;
various time, temp.;
|
29 % Chromat. 44 % Chromat. 17 % Chromat. 8 % Chromat. |
1,2-dimethoxy-4-(2-propenyl)benzene
Methylisoeugenol
Conditions | Yield |
---|---|
With
potassium hydroxide;
In
butan-1-ol;
for 12h;
Reflux;
|
86% |
With
potassium carbonate;
|
|
With
bis(cyclopentadienyl)titanium dichloride; ethylaluminum dichloride; magnesium;
In
tetrahydrofuran;
at 0 - 22 ℃;
for 72h;
Inert atmosphere;
Schlenk technique;
|
|
With
[{RuCl(μ-Cl)(η3:η3-2,7-dimethylocta-2,6-diene-1,8-diyl)}2];
In
methanol; water;
at 80 ℃;
for 1.5h;
|
1,2-dimethoxy-4-(2-propenyl)benzene
1-(3,4-dimethoxyphenyl)propan-1-ol
ethylmagnesium iodide
3,4-dimethoxy-benzaldehyde
1-(3,4-dimethoxyphenyl)-2-nitropropene
6,7-dimethoxy-3-methyl-1-phenyl-3,4-dihydro-isoquinoline
6,7-dimethoxy-3-methyl-3,4-dihydro-isoquinoline; hydrochloride
4-(3,4-dimethoxy-phenyl)-5-methyl-[1,3]dioxane
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