CAS 27407-11-0
:3-Bromo-4-fluorophenol
Description:
3-Bromo-4-fluorophenol is an organic compound characterized by the presence of both bromine and fluorine substituents on a phenolic ring. Specifically, the bromine atom is located at the meta position (3-position) and the fluorine atom at the para position (4-position) relative to the hydroxyl (-OH) group. This compound typically appears as a solid or liquid, depending on the temperature and purity, and is known for its potential applications in pharmaceuticals and agrochemicals due to its reactivity and ability to participate in various chemical reactions. The presence of both halogens can influence the compound's physical properties, such as solubility and boiling point, as well as its chemical reactivity, making it a valuable intermediate in organic synthesis. Additionally, 3-Bromo-4-fluorophenol may exhibit specific biological activities, which can be of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C6H4BrFO
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
3-Bromo-4-fluorophenol, 98%
CAS:<p>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 Sci</p>Formula:C6H4BrFOPurity:98%Molecular weight:191.003-Bromo-4-fluorophenol
CAS:Formula:C6H4BrFOPurity:>99.0%(GC)(T)Color and Shape:Light orange to Yellow to Green powder to crystalMolecular weight:191.003-Bromo-4-fluorophenol
CAS:<p>3-Bromo-4-fluorophenol</p>Formula:C6H4BrFOPurity:97%Color and Shape: light yellow to yellow solidMolecular weight:191.00g/mol3-Bromo-4-fluorophenol
CAS:<p>3-Bromo-4-fluorophenol is a synthetic, water soluble, and stable compound with a variety of applications. It yields white crystals that are soluble in water, acetone, ethanol, ether, benzene, chloroform, and carbon tetrachloride. 3-Bromo-4-fluorophenol has been shown to have a number of structural modifications that may be advantageous for therapeutic purposes. The most prominent modification is the methylation of the phenolic hydroxyl group (functionalisation). This modification prevents the drug from reacting with nucleophilic sites on proteins and other biological molecules. 3-Bromo-4-fluorophenol interacts with methyltransferase enzymes in cancer cells to inhibit their activity. These methyltransferase enzymes are involved in cellular proliferation and proliferation signalling pathways that may lead to cancer cell death.</p>Formula:C6H4BrFOPurity:Min. 95%Color and Shape:PowderMolecular weight:191 g/mol
