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CAS 871332-98-8

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

Description:
B-(5-Bromo-2-ethoxy-3-pyridinyl)boronic acid, with the CAS number 871332-98-8, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a pyridine ring. 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 Suzuki coupling reactions. The presence of the bromine atom enhances its reactivity and can facilitate further functionalization. The ethoxy group contributes to its solubility in organic solvents and may influence its electronic properties. Additionally, the pyridine moiety can participate in coordination chemistry, potentially interacting with metal ions. Overall, this compound is of interest in medicinal chemistry and materials science due to its unique structural features and reactivity profile. Safety precautions should be observed when handling this compound, as with all boronic acids, due to potential toxicity and environmental concerns.
Formula:C7H9BBrNO3
InChI:InChI=1/C7H9BBrNO3/c1-2-13-7-6(8(11)12)3-5(9)4-10-7/h3-4,11-12H,2H2,1H3
InChI key:InChIKey=VXXXKWUXSALQQW-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OCC)N=CC(Br)=C1
Synonyms:
  • (5-Bromo-2-ethoxypyridin-3-yl)boronic acid
  • B-(5-Bromo-2-ethoxy-3-pyridinyl)boronic acid
  • Boronic acid, (5-bromo-2-ethoxy-3-pyridinyl)-
  • boronic acid, B-(5-bromo-2-ethoxy-3-pyridinyl)-
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