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CAS 850567-93-0

:

B-(2,6-Dibromo-3-methoxyphenyl)boronic acid

Description:
B-(2,6-Dibromo-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 two bromine atoms and a methoxy group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar organic solvents. 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 bromine atoms enhances its reactivity and potential for further functionalization, while the methoxy group can influence the electronic properties of the molecule, affecting its reactivity and solubility. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including sensor technology and drug delivery systems. Overall, this compound is significant in the field of synthetic organic chemistry due to its versatile reactivity and functional group compatibility.
Formula:C7H7BBr2O3
InChI:InChI=1S/C7H7BBr2O3/c1-13-5-3-2-4(9)6(7(5)10)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=CCRLWBYZCYCUAK-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Br)C(OC)=CC=C1Br
Synonyms:
  • (2,6-Dibromo-3-methoxyphenyl)boronic acid
  • 2,6-Dibromo-3-methoxyphenylboronic acid
  • B-(2,6-Dibromo-3-methoxyphenyl)boronic acid
  • Boronic acid, (2,6-dibromo-3-methoxyphenyl)-
  • Boronicacid, (2,6-dibromo-3-methoxyphenyl)- (9CI)
  • Boronic acid, B-(2,6-dibromo-3-methoxyphenyl)-
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