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CAS 1072952-51-2

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B-(2-Bromo-5-chloro-4-pyridinyl)boronic acid

Description:
B-(2-Bromo-5-chloro-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that is substituted with both bromine and chlorine atoms. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents can influence its reactivity and solubility, potentially enhancing its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds. Additionally, the pyridine moiety may impart specific electronic properties, affecting the compound's behavior in biological systems or its interaction with other chemical species. Overall, B-(2-Bromo-5-chloro-4-pyridinyl)boronic acid is a versatile compound with significant relevance in synthetic organic chemistry and drug development.
Formula:C5H4BBrClNO2
InChI:InChI=1S/C5H4BBrClNO2/c7-5-1-3(6(10)11)4(8)2-9-5/h1-2,10-11H
InChI key:InChIKey=OEBDNRIHMPUZNU-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(Cl)=CN=C(Br)C1
Synonyms:
  • 2-Bromo-5-chloropyridine-4-boronic acid
  • B-(2-Bromo-5-chloro-4-pyridinyl)boronic acid
  • (2-Bromo-5-chloropyridin-4-yl)boronic acid
  • Boronic acid, B-(2-bromo-5-chloro-4-pyridinyl)-
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