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CAS 612845-46-2

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(5-Bromo-2-ethoxypyridin-4-yl)boronicacid

Description:
(5-Bromo-2-ethoxypyridin-4-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. The compound features a bromine atom at the 5-position and an ethoxy group at the 2-position of the pyridine, which contributes to its unique reactivity and solubility properties. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in Suzuki coupling reactions for the formation of carbon-carbon bonds. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its reactivity can be influenced by the presence of the bromine and ethoxy substituents, which can affect its electronic properties and steric hindrance. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, which can lead to hydrolysis and loss of the boronic acid functionality.
Formula:C7H9BBrNO3
InChI:InChI=1S/C7H9BBrNO3/c1-2-13-7-3-5(8(11)12)6(9)4-10-7/h3-4,11-12H,2H2,1H3
SMILES:CCOc1cc(c(cn1)Br)B(O)O
Synonyms:
  • (5-bromo-2-ethoxypyridin-4-yl)boronicaci
  • 5-BROMO-2-ETHOXYPYRIDINE-4-BORONIC ACID
  • Boronic acid, (5-broMo-2-ethoxy-4-pyridinyl)- (9CI)
  • 5-BROMO-2-ETHOXY-4-PYRIDINEBORONIC ACID
  • (5-Bromo-2-ethoxy-4-pyridinyl)-boronic acid
  • 5-BROMO-2-ETHOXYPYRIDIN-4-YLBORONIC ACID
  • (5-Bromo-2-ethoxy-4-pyridyl)boronic acid
  • (3-Bromo-5-ethoxypyridin-4-yl)boronic acid
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