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CAS 957062-85-0

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B-(4-Bromo-6-chloro-3-pyridinyl)boronic acid

Description:
B-(4-Bromo-6-chloro-3-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 bromine and chlorine atoms. This compound typically exhibits properties common to 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 (bromine and chlorine) on the pyridine ring can influence its reactivity and solubility, potentially enhancing its biological activity or selectivity in chemical reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's structure suggests it may also exhibit specific interactions with biological targets, making it of interest in drug discovery and development. Overall, B-(4-Bromo-6-chloro-3-pyridinyl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C5H4BBrClNO2
InChI:InChI=1S/C5H4BBrClNO2/c7-4-1-5(8)9-2-3(4)6(10)11/h1-2,10-11H
InChI key:InChIKey=LFWCFEIUOQWFAY-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(Br)=CC(Cl)=NC1
Synonyms:
  • Boronic acid, B-(4-bromo-6-chloro-3-pyridinyl)-
  • B-(4-Bromo-6-chloro-3-pyridinyl)boronic acid
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