
CAS 766-85-8: 3-Iodoanisole
Formula:C7H7IO
InChI:InChI=1S/C7H7IO/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3
InChI key:InChIKey=RSHBAGGASAJQCH-UHFFFAOYSA-N
SMILES:O(C)C1=CC(I)=CC=C1
Synonyms:- 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
- m-Methoxyiodobenzene
- m-Methoxyphenyl iodide
- See more synonyms
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Found 9 products.
3-Iodoanisole, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C7H7IOPurity:97%Color and Shape:Clear yellow, Liquid, May darken on storageMolecular weight:234.043-Iodoanisole
CAS:Controlled ProductApplications 3-Iodoanisole (cas# 766-85-8) is a compound useful in organic synthesis.Formula:C7H7IOColor and Shape:NeatMolecular weight:234.033-Iodoanisole, 98%
CAS:3-Iodoanisole is used to produce 3,3'-Dimethoxy-biphenyl. It can be used in agrochemical, pharmaceutical and dyestuff field. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C7H7IOPurity:98%Color and Shape:Clear colorless to yellow, LiquidMolecular weight:234.043-Iodoanisole
CAS:Formula:C7H7IOPurity:(GC) ≥ 97.0%Color and Shape:Light yellow to yellow liquidMolecular weight:234.043-Iodoanisole
CAS: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.Formula:C7H7IOPurity:Min. 98 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:234.03 g/mol3-Iodoanisole
CAS:Formula:C7H7IOPurity:>98.0%(GC)Color and Shape:Colorless to Yellow to Green clear liquidMolecular weight:234.04