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CAS 1451391-70-0

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

Description:
B-(5-Bromo-3-chloro-2-ethoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with both bromine and chlorine atoms, contributing to its reactivity and potential for further functionalization. The ethoxy group enhances its solubility in organic solvents, facilitating its use in various chemical reactions. Boronic acids are typically used in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The presence of halogen substituents can also influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with other chemical species. Overall, B-(5-Bromo-3-chloro-2-ethoxyphenyl)boronic acid is a versatile compound with significant implications in synthetic organic chemistry and materials science.
Formula:C8H9BBrClO3
InChI:InChI=1S/C8H9BBrClO3/c1-2-14-8-6(9(12)13)3-5(10)4-7(8)11/h3-4,12-13H,2H2,1H3
InChI key:InChIKey=CBQUBIYNGMJEAW-UHFFFAOYSA-N
SMILES:O(CC)C1=C(B(O)O)C=C(Br)C=C1Cl
Synonyms:
  • B-(5-Bromo-3-chloro-2-ethoxyphenyl)boronic acid
  • Boronic acid, B-(5-bromo-3-chloro-2-ethoxyphenyl)-
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