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CAS 2121511-66-6

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

Description:
B-(2-Bromo-5-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 organic synthesis applications, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The presence of halogen substituents (bromine and chlorine) on the pyridine ring can influence its reactivity and solubility, as well as its potential biological activity. Additionally, boronic acids are known for their role in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. The compound's structure suggests it may have applications in agrochemicals or as a building block in the synthesis of more complex molecules. As with all chemical substances, handling should be conducted with appropriate safety measures due to potential toxicity and reactivity.
Formula:C5H4BBrClNO2
InChI:InChI=1S/C5H4BBrClNO2/c7-5-4(6(10)11)1-3(8)2-9-5/h1-2,10-11H
InChI key:InChIKey=BGSVCRJTLJKVJJ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Br)N=CC(Cl)=C1
Synonyms:
  • Boronic acid, B-(2-bromo-5-chloro-3-pyridinyl)-
  • B-(2-Bromo-5-chloro-3-pyridinyl)boronic acid
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