1-Fluoro-3,5-dimethoxybenzene, 98%, Thermo Scientific Chemicals
Element SearchElement SearchStructure SearchStructure Search
1-Fluoro-3,5-dimethoxybenzene, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

1-Fluoro-3,5-dimethoxybenzene, 98%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
5 g
100 g
ChemDexTry the chem dexTM web app
Catalog number B24810.14
also known as B24810-14
Price (TWD)/ Each
-
Request A Quote
Quantity:
25 g
Request bulk or custom format
Chemical Identifiers
CAS52189-63-6
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥97.5%
FormLiquid
Refractive Index1.5005-1.5045 @ 20?C
1-Fluoro-3,5-dimethoxybenzene is used in the preparation of 5-fluoro-benzene-1,3-diol using reagents like tetrabutylammnoium iodide and boron trichloirde.

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.

Applications
1-Fluoro-3,5-dimethoxybenzene is used in the preparation of 5-fluoro-benzene-1,3-diol using reagents like tetrabutylammnoium iodide and boron trichloirde.

Solubility
Slightly miscible with water.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Geier, M. J.; Aseman, M. D.; Gagné, M. R. Anion-Dependent Switch in C-X Reductive Elimination Diastereoselectivity. Organometallics 2014, 33 (17), 4353-4356.
  2. Su, D. S.; Lim, J. J.; Tinney, E.; Wan, B. L.; Young, M. B.; Anderson, K. D.; Rudd, D.; Munshi, V.; Bahnck, C.; Felock, P. J.; Lu, M.; Lai, M. T.; Touch, S.; Moyer, G.; DiStefano, D. J.; Flynn, J. A.; Liang, Y.; Sanchez, R.; Perlow-Poehnelt, R.; Miller, M.; Vacca, J. P.; Williams, T. M.; Anthony, N. J. Biaryl ethers as novel non-nucleoside reverse transcriptase inhibitors with improved potency against key mutant viruses. J. Med. Chem. 2009, 52 (22), 7163-7169.