CAS 2121511-62-2
:B-(4-Bromo-3,5-dichlorophenyl)boronic acid
Description:
B-(4-Bromo-3,5-dichlorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with bromine and chlorine atoms. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The presence of halogen substituents, specifically bromine and chlorine, can influence its reactivity and stability, making it useful in various chemical reactions, including Suzuki coupling reactions for the formation of carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug design. The compound's unique structure and functional properties make it valuable in organic synthesis and materials science, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C6H4BBrCl2O2
InChI:InChI=1S/C6H4BBrCl2O2/c8-6-4(9)1-3(7(11)12)2-5(6)10/h1-2,11-12H
InChI key:InChIKey=FIIAWVYUPICPON-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(Cl)=C(Br)C(Cl)=C1
Synonyms:- Boronic acid, B-(4-bromo-3,5-dichlorophenyl)-
- B-(4-Bromo-3,5-dichlorophenyl)boronic acid
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