CAS 849062-37-9
:3-Bromo-5-fluorophenylboronic acid
Description:
3-Bromo-5-fluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both bromine and fluorine atoms. This compound typically exhibits a white to off-white crystalline solid form and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group. The presence of the bromine and fluorine substituents can influence its reactivity and interactions, making it useful in various chemical applications, including Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. Additionally, the boronic acid functionality allows for the formation of reversible complexes with diols, which can be exploited in sensor technologies and drug delivery systems. Its unique electronic properties, derived from the halogen substituents, can also affect its behavior in biological systems and materials science. Overall, 3-Bromo-5-fluorophenylboronic acid is a versatile compound with significant utility in synthetic organic chemistry and related fields.
Formula:C6H5BBrFO2
InChI:InChI=1/C6H5BBrFO2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,10-11H
SMILES:c1c(cc(cc1Br)F)B(O)O
Synonyms:- 3-Bromo-5-fluorobenzeneboronic acid
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Found 3 products.
3-Bromo-5-fluorophenylboronic acid
CAS:Formula:C6H5BBrFO2Purity:98%Color and Shape:SolidMolecular weight:218.81613-Bromo-5-fluorobenzeneboronic acid
CAS:<p>3-Bromo-5-fluorobenzeneboronic acid</p>Purity:95%Color and Shape:Pale Yellow CrystalsMolecular weight:218.82g/mol(3-Bromo-5-fluorophenyl)boronic acid
CAS:Formula:C6H5BBrFO2Purity:98%Color and Shape:SolidMolecular weight:218.82


