Introduction：Basic information about 2-methoxy-4-prop-1-enylphenetole CAS 7784-67-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
2-methoxy-4-prop-1-enylphenetole Basic information
| Product Name: | 2-methoxy-4-prop-1-enylphenetole |
| Synonyms: | 2-methoxy-4-prop-1-enylphenetole;Ethyl-iso-eugenol;Benzene, 1-ethoxy-2-methoxy-4-(1-propenyl)-;ISOEUGENYLETHYLETHER;Ethyl isoeugenyl ether;2-Methoxy-4-(1-propenyl)phenylethyl ether;Benzene, 1-ethoxy-2-Methoxy-4-(1-propen-1-yl)-;isoeugenyl ether ether |
| CAS: | 7784-67-0 |
| MF: | C12H16O2 |
| MW: | 192.25 |
| EINECS: | 232-072-6 |
| Product Categories: | |
| Mol File: | 7784-67-0.mol |
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2-methoxy-4-prop-1-enylphenetole Chemical Properties
| FEMA | 2472 | ISOEUGENYL ETHYL ETHER |
| solubility | Practically insoluble in water, soluble in alcohol and oils. |
| form | White or colourless crystals. |
| Odor | at 100.00 %. spicy carnation clove |
| Odor Type | spicy |
| JECFA Number | 1267 |
| LogP | 3.58 |
| EPA Substance Registry System | Benzene, 1-ethoxy-2-methoxy-4-(1-propenyl)- (7784-67-0) |
Safety Information
2-methoxy-4-prop-1-enylphenetole Usage And Synthesis
| Description | Isoeugenyl ethyl ether has an odor similar to isoeugenol. Preparedfrom isoeugenol by boiling with ethyl p-toluenesulfonate. |
| Chemical Properties | Isoeugenyl ethyl ether has an odor similar to isoeugenol. |
| Uses | Ethylisoeugenol is a prenylated dehydrozingerone analog, a potent potential chemopreventive agent for cancer. |
| Application | 2-methoxy-4-prop-1-enylphenetole is an excellent sweetener, stable in soap, and it does not discolour in cosmetic preparations as easily as Eugenol, Vanillin, etc. 2-methoxy-4-prop-1-enylphenetole may meanwhile become a popular fragrance chemical for its very pleasant effect and great tenacity. It blends very well with Oakmoss, Ylang, Methylionones, Patchouli, Coumarins, etc. However, cosmetic skin research is very concerned about the Propenyl group, which is accused of being a hazard to the human skin, which would bring Eugenolderivatives under the limelight and possibly ban them from use in cosmetic fragrances. |
| Preparation | From isoeugenol by boiling with ethyl p-toluenesulfonate. |
| Synthesis Reference(s) | Synthetic Communications, 20, p. 345, 1990 DOI: 10.1080/00397919008052774 |
2-methoxy-4-prop-1-enylphenetole Preparation Products And Raw materials
| Preparation Products | ISOEUGENOL |
