Product Information
- 1-Iodo-3-methoxy-benzene1-Iodo-3-methoxybenzene3-Methoxyphenyl iodide
- 1-Iodo-3-Methoxybenzene
- 3-Iodophenyl methyl ether
- 3-Methoxy-1-iodobenzene
- 3-Methoxyiodobenzene
- 3-Methoxyphenyl iodide
- Anisole, m-iodo-
- Benzene, 1-iodo-3-methoxy-
- NSC 60726
- m-Iodoanisole
- See more synonyms
- m-Methoxyiodobenzene
- m-Methoxyphenyl iodide
3-Iodoanisole is a reactive aryl halide that undergoes the Friedel-Crafts reaction with carbamic acid to produce anisole. The rate of this reaction is increased by the addition of nitrous acid, which is used as a catalyst. 3-Iodoanisole has two stereoisomers, one of which is more reactive than the other. This reactivity can be explained by electron-donating and electron-withdrawing effects on the substituents on the ring. The functional theory states that nucleophilic attack occurs at the carbon atom with least steric hindrance. 3-Iodoanisole reacts faster in hexane than in methanol because it has a lower boiling point and higher solubility in hexane.
Chemical properties
Technical inquiry about: 3D-FI24613 3-Iodoanisole
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