| Weight | 234.036 g/mol |
|---|---|
| Formula | C7H7IO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
4-Iodoanisole (696-62-8)
Izoform
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- Synthesis of a Chiral Precursor for No-Carrier-Added (NCA) PET Tracer 6-[18F]Fluoro-L-dopa Based on Regio- and Enantioselective Alkylation of 2,4-Bis(chloromethyl)-5-iodoanisole (Bulletin of the Chemical Society of Japan, 2000)
- The Heck Reaction of N-Protected Vinylglycines with 4-Iodoanisole (Chemical & Pharmaceutical Bulletin, 1995)
- Oxidative and non-oxidative metabolism of 4-iodoanisole by rat liver microsomes (Xenobiotica, 1995)
- Palladium catalyzed cross-coupling of (Z)-1-heptenyldimethylsilanol with 4-iodoanisole: (Z)-1-Heptenyl-4-methoxybenzene: [Benzene,1-(1Z)-1-heptenyl-4-methoxy-] (Organic Syntheses, 2005)
- Mechanism of iodine migration during the nitrodeiodination of 4-iodoanisole (Journal of The Chemical Society-perkin Transactions 1, 1972)
- Nitration of 3-iodoanisole and 2,6-dimethyl-4-iodoanisole (Journal of The Chemical Society-perkin Transactions 1, 1974)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Izoform
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SMILESCOC1=CC=C(C=C1)I
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InChIKeySYSZENVIJHPFNL-UHFFFAOYSA-N
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4-Iodoanisole
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