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CAS 1256355-39-1

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

Description:
B-(4-Bromo-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 a bromine atom. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The presence of the bromine atom enhances its reactivity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, where it serves as a key building block for the synthesis of biaryl compounds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including drug delivery and sensor technology. The compound's unique structure and reactivity profile make it valuable in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and advanced materials.
Formula:C5H5BBrNO2
InChI:InChI=1S/C5H5BBrNO2/c7-5-1-2-8-3-4(5)6(9)10/h1-3,9-10H
InChI key:InChIKey=OEQUZDNRPMTXMQ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(Br)=CC=NC1
Synonyms:
  • Boronic acid, B-(4-bromo-3-pyridinyl)-
  • B-(4-Bromo-3-pyridinyl)boronic acid
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