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CAS 957035-13-1

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(2-bromo-6-ethoxy-phenyl)boronic acid

Description:
(2-Bromo-6-ethoxy-phenyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a bromine atom and an ethoxy group attached to a phenyl ring, contributing to its reactivity and solubility properties. Typically, boronic acids are polar and can participate in various chemical reactions, including Suzuki coupling, which is essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. The presence of the ethoxy group enhances its solubility in organic solvents, while the bromine atom can serve as a leaving group in substitution reactions. Additionally, (2-bromo-6-ethoxy-phenyl)boronic acid may exhibit unique properties such as pH sensitivity and potential biological activity, making it a valuable compound in pharmaceutical research and development. Its specific applications and behavior can vary based on the surrounding chemical environment and conditions.
Formula:C8H10BBrO3
InChI:InChI=1/C8H10BBrO3/c1-2-13-7-5-3-4-6(10)8(7)9(11)12/h3-5,11-12H,2H2,1H3
SMILES:CCOc1cccc(c1B(O)O)Br
Synonyms:
  • (2-Bromo-6-ethoxyphenyl)boronic acid
  • boronic acid, B-(2-bromo-6-ethoxyphenyl)-
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