CAS 529-28-2
:2-Iodoanisole
- 1-Iodo-2-Methoxy-Benzen
- 1-Iodo-2-Methoxybenzene
- 2-Iodoanisole 97%
- 2-Iodoanisole,99%
- 2-Iodoanisole97%
- 2-Iodophenyl Methyl Ether
- 2-Methoxy-1-iodobenzene
- 2-Methoxyiodobenzene
- 2-Methoxyphenyl iodide
- Anisole, o-iodo-
- Benzene, 1-iodo-2-methoxy-
- Iodanisol
- NSC 9259
- O-Iodoanisole
- o-Anisyl iodide
- o-Iodomethoxybenzene
- o-Methoxyiodobenzene
- o-Methoxyphenyl iodide
- 2-Iodoanisole
- 2-Iodo-1-methoxybenzene
- 1-Methoxy-2-iodobenzene
- 2-IODOANISOLE/1-IODO-2-METHOXYBENZENE
- 2-Iodoanisole (stabilized with Copper chip)
- 2-Iodophenyl methyl ether, 2-Methoxyiodobenzene
- See more synonyms
2-Iodoanisole, 99%
CAS:2-Iodoanisole has been used in palladium/copper-catalyzed synthesis of o-(1-alkynyl)anisoles. 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 produc
Formula:C7H7IOPurity:99%Color and Shape:Clear pale yellow to yellow, LiquidMolecular weight:234.042-Iodoanisole
CAS:2-IodoanisolePurity:98%Color and Shape:Pale Yellow LiquidMolecular weight:234.03g/mol2-Iodoanisole (stabilized with Copper chip)
CAS:Formula:C7H7IOPurity:>98.0%(GC)Color and Shape:White to Yellow to Green clear liquidMolecular weight:234.041-Iodo-2-methoxybenzene
CAS:1-Iodo-2-methoxybenzene is a compound that has shown to have anti-cancer properties. It is an effective inhibitor of protein tyrosine kinases, which are involved in the activation of inflammatory diseases and cancer. The hydroxyl group on the benzenoid ring activates the molecule by hydrogen bonding with the protein target, thereby inhibiting its activity. 1-Iodo-2-methoxybenzene may also be used as a contrast agent for magnetic resonance imaging (MRI) due to its light emission properties.
Formula:C7H7IOPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:234.03 g/mol2-Iodoanisole
CAS:Controlled ProductApplications 2-Iodoanisole is a useful synthetic intermediate. It can be used in the synthesis of piperidinyl diaminopyrimidines as cyclin-dependent kinase inhibitors with antitumor activity and polysubstituted benzofuran derivatives as novel inhibitors of parasitic growth.
References Chu, X., et al.: J. Med. Chem., 49, 6549 (2006); Thevenin, M., et al.: Bioorg. Med. Chem., 21, 4885 (2013)Formula:C7H7IOColor and Shape:NeatMolecular weight:234.03







