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CAS 1072944-19-4

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

Description:
B-(5-Bromo-2-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 both 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 can enhance its reactivity and influence its interactions with biological targets. Additionally, the pyridine ring contributes to the compound's aromaticity and potential for coordination with metal ions. B-(5-Bromo-2-chloro-3-pyridinyl)boronic acid may also exhibit solubility in polar organic solvents, and its reactivity can be modulated by the electronic effects of the halogen substituents. Overall, this compound is of interest in the development of pharmaceuticals and as a building block in the synthesis of more complex organic molecules.
Formula:C5H4BBrClNO2
InChI:InChI=1S/C5H4BBrClNO2/c7-3-1-4(6(10)11)5(8)9-2-3/h1-2,10-11H
InChI key:InChIKey=VDOTXMKSABQXLA-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)N=CC(Br)=C1
Synonyms:
  • B-(5-Bromo-2-chloro-3-pyridinyl)boronic acid
  • Boronic acid, B-(5-bromo-2-chloro-3-pyridinyl)-
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