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CAS 957062-55-4

:

B-(6-Bromo-2-chloro-3-methoxyphenyl)boronic acid

Description:
B-(6-Bromo-2-chloro-3-methoxyphenyl)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, chlorine, and methoxy groups. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard laboratory conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of halogen substituents can influence its reactivity and interaction with biological targets. Additionally, the methoxy group can enhance solubility and modulate electronic properties, affecting the compound's overall behavior in chemical reactions. As with many boronic acids, it may also exhibit pH-dependent solubility and reactivity, which is important for its application in various chemical processes. Safety data should be consulted for handling and disposal, as with all chemical substances.
Formula:C7H7BBrClO3
InChI:InChI=1S/C7H7BBrClO3/c1-13-5-3-2-4(9)6(7(5)10)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=YITPGJUOVXQLPQ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(OC)=CC=C1Br
Synonyms:
  • Boronic acid, B-(6-bromo-2-chloro-3-methoxyphenyl)-
  • (6-Bromo-2-chloro-3-methoxyphenyl)boronic acid
  • B-(6-Bromo-2-chloro-3-methoxyphenyl)boronic acid
  • (6-Bromo-2-chloro-3-methoxyphenyl)boronicacid
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