CAS 957034-55-8
:[2-bromo-5-(trifluoromethoxy)phenyl]boronic acid
Description:
[2-Bromo-5-(trifluoromethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a bromine atom and a trifluoromethoxy group attached to a phenyl ring, contributing to its unique reactivity and solubility properties. The trifluoromethoxy group enhances the electron-withdrawing characteristics of the molecule, potentially increasing its acidity and reactivity in nucleophilic substitution reactions. This compound is typically used in organic synthesis and medicinal chemistry, where it can serve as a building block for more complex molecules. Additionally, its boronic acid moiety allows for the formation of stable complexes with biomolecules, making it of interest in drug development and materials science. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C7H5BBrF3O3
InChI:InChI=1/C7H5BBrF3O3/c9-6-2-1-4(15-7(10,11)12)3-5(6)8(13)14/h1-3,13-14H
SMILES:c1cc(c(cc1OC(F)(F)F)B(O)O)Br
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
2-Bromo-5-(trifluoromethoxy)benzeneboronic acid
CAS:2-Bromo-5-(trifluoromethoxy)benzeneboronic acidFormula:C7H5BBrF3O3Purity:96%Color and Shape: off white solidMolecular weight:284.82g/mol(2-Bromo-5-(trifluoromethoxy)phenyl)boronic acid
CAS:Formula:C7H5BBrF3O3Purity:95.0%Color and Shape:SolidMolecular weight:284.82


