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CAS 957060-94-5

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

Description:
B-(5-Bromo-2-methoxy-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 a bromine atom and a methoxy group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in polar solvents like water and alcohols due to the presence of the boronic acid group. It is often used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are valuable for forming carbon-carbon bonds. The bromine substituent enhances its reactivity, while the methoxy group can influence the electronic properties of the pyridine ring. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.
Formula:C6H7BBrNO3
InChI:InChI=1S/C6H7BBrNO3/c1-12-6-2-4(7(10)11)5(8)3-9-6/h2-3,10-11H,1H3
InChI key:InChIKey=ZNJUFOAOSUTWIG-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(OC)N=CC1Br
Synonyms:
  • (5-Bromo-2-methoxy-4-pyridyl)boronic acid
  • (5-Bromo-2-methoxypyridin-4-yl)boronic acid
  • 5-Bromo-2-Methoxypyridin-4-Ylboronic Acid
  • B-(5-Bromo-2-methoxy-4-pyridinyl)boronic acid
  • Boronic acid, B-(5-bromo-2-methoxy-4-pyridinyl)-
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