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CAS 2096341-68-1

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B-(3-Bromo-5-chloro-2-methoxyphenyl)boronic acid

Description:
B-(3-Bromo-5-chloro-2-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The compound features a bromine atom and a chlorine atom as substituents on the aromatic ring, along with a methoxy group, which contributes to its chemical reactivity and solubility properties. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents can enhance the compound's reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in the formation of carbon-carbon bonds. Additionally, the methoxy group can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with biological targets. Overall, B-(3-Bromo-5-chloro-2-methoxyphenyl)boronic acid is a versatile compound with significant implications in synthetic organic chemistry and drug development.
Formula:C7H7BBrClO3
InChI:InChI=1S/C7H7BBrClO3/c1-13-7-5(8(11)12)2-4(10)3-6(7)9/h2-3,11-12H,1H3
InChI key:InChIKey=RLBSHQKQVPRDPZ-UHFFFAOYSA-N
SMILES:O(C)C1=C(B(O)O)C=C(Cl)C=C1Br
Synonyms:
  • B-(3-Bromo-5-chloro-2-methoxyphenyl)boronic acid
  • Boronic acid, B-(3-bromo-5-chloro-2-methoxyphenyl)-
  • (3-Bromo-5-chloro-2-mthoxyphnyl)boronic acid
  • 3-Bromo-5-chloro-2-methoxyphenylboronic acid
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