CAS 1451392-94-1
:B-(3-Bromo-2,6-dichlorophenyl)boronic acid
Description:
B-(3-Bromo-2,6-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 properties such as being a white to off-white solid, with moderate solubility in polar solvents like water and alcohols, due to the presence of the boronic acid group. It is often utilized in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The presence of halogen substituents can enhance its reactivity and selectivity in various chemical transformations. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensing applications. Safety considerations should be taken into account when handling this compound, as it may pose hazards typical of organoboron compounds, including potential toxicity and environmental concerns.
Formula:C6H4BBrCl2O2
InChI:InChI=1S/C6H4BBrCl2O2/c8-3-1-2-4(9)5(6(3)10)7(11)12/h1-2,11-12H
InChI key:InChIKey=ZRMOEVKPJFFEND-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(Br)=CC=C1Cl
Synonyms:- B-(3-Bromo-2,6-dichlorophenyl)boronic acid
- Boronic acid, B-(3-bromo-2,6-dichlorophenyl)-
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