| Weight | 148.205 g/mol |
|---|---|
| Formula | C10H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
cis-Anethole
4180-23-8, 25679-28-1, 104-46-1
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- Electron transfer induced photoisomerization, dimerization, and oxygenation of trans- and cis-anethole: the role of monomer and dimer cation radicals (Journal of the American Chemical Society, 1988)
- Photodimerization of singlet trans- and cis-anethole: concerted or stepwise? (Journal of the American Chemical Society, 1988)
- Acid-catalyzed hydrolysis of cis- and trans-anethole oxides : discrete carbocation intermediates and Syn/anti hydration ratios (Journal of Organic Chemistry, 1993)
- PHOTOINDUCED ELECTRON TRANSFER REACTIONS OF ARYL OLEFINS. II: CIS-TRANS ISOMERIZATION AND CYCLOADDUCT FORMATION IN ANETHOLE-FUMARONITRILE SYSTEMS IN P OLAR SOLVENTS (Journal of the American Chemical Society, 1996)
- Reactions of sulfenyl chlorides and their derivatives. VII. Nonstereospecific addition of 2,4-dinitrobenzenesulfenyl chloride to cis- and trans-anethole (Journal of Organic Chemistry, 1972)
- Spontaneous hydrolysis reactions of cis- and trans-beta-methyl-4-methoxystyrene oxides (Anethole oxides): buildup of trans-anethole oxide as an intermediate in the spontaneous reaction of cis-anethole oxide. (Journal of Organic Chemistry, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC=CC1=CC=C(C=C1)OC
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InChIKeyRUVINXPYWBROJD-UHFFFAOYSA-N
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