| Weight | 234.036 g/mol |
|---|---|
| Formula | C7H7IO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Iodoanisole (529-28-2)
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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)
- Nitration of 3-iodoanisole and 2,6-dimethyl-4-iodoanisole (Journal of The Chemical Society-perkin Transactions 1, 1974)
- ChemInform Abstract: NITRATION OF 3-IODOANISOLE AND 2,6-DIMETHYL-4-IODOANISOLE (ChemInform, 1975)
- Syntheses of 2,3-Difluoro-4-iodoanisole (Fine chemicals, 2006)
- ChemInform Abstract: Synthesis of a Chiral Precursor for NoCarrierAdded (NCA) PET Tracer 6[18F]FluoroLdopa Based on Regio and Enantioselective Alkylation of 2,4Bis(chloromethyl)5iodoanisole. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC=CC=C1I
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InChIKeyDVQWNQBEUKXONL-UHFFFAOYSA-N
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Similar Compounds
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(103-73-1)
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2-Iodoanisole
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