CAS 321-28-8
:2-Fluoroanisole
- 1-Fluoro-2-Methoxybenzene
- 2-Fluoro-1-methoxybenzene
- 2-Fluoromethoxybenzene
- 2-Methoxyfluorobenzene
- 6-fluoro-4H-1,3-benzodioxine-8-carboxylic acid
- Anisole, o-fluoro-
- Benzene, 1-fluoro-2-methoxy-
- NSC 10339
- O-Fluoroanisole
- 2-Fluoroanisole
2-Fluoroanisole
CAS:Formula:C7H7FOPurity:>96.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:126.131-Fluoro-2-methoxybenzene
CAS:Formula:C7H7FOPurity:98%Color and Shape:LiquidMolecular weight:126.12832-Fluoroanisole
CAS:2-FluoroanisoleFormula:C7H7FOPurity:99%Color and Shape: clear liquidMolecular weight:126.13g/mol2-Fluoroanisole
CAS:Controlled ProductApplications 2-Fluoroanisole is a useful synthetic intermediate with antifungal activity.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Pinto, M. F. S., et al.: J. Mol. Struc.: Theochem., 539, 303-310 (2001)Formula:C7H7FOColor and Shape:NeatMolecular weight:126.132-Fluoroanisole
CAS:2-Fluoroanisole is an organic compound that is used in organic synthesis as a chiral auxiliary. It has been shown to inhibit the growth of cancer cells by binding to nucleophilic sites on the cell and preventing the formation of new proteins. 2-fluoroanisole is synthesized through a two-step process that begins with the asymmetric synthesis of the desired chiral molecule using a chiral catalyst and deuterium isotope. The second step involves converting 2-fluoroanisole into its more stable form, dodecanedioic acid, by treating it with hydrochloric acid or trifluoroacetic acid. The structural analysis of this molecule revealed that it contains two nucleophilic substitutions, which are likely responsible for its inhibitory properties.
Formula:C7H7FOPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:126.13 g/mol2-Fluoroanisole pure, 98%
CAS:Formula:FC6H4OCH3Purity:min. 98%Color and Shape:Clear, Colourless to pale yellow, LiquidMolecular weight:126.13







