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CAS 913835-87-7

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(3-bromo-5-methoxycarbonyl-phenyl)boronic acid

Description:
(3-Bromo-5-methoxycarbonyl-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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a bromine atom and a methoxycarbonyl group attached to a phenyl ring, contributing to its reactivity and solubility properties. The presence of the boronic acid group imparts acidity, allowing it to participate in acid-base reactions. This compound is typically used in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structural features suggest potential applications in materials science and catalysis. Additionally, the bromine substituent can serve as a leaving group in nucleophilic substitution reactions, enhancing its utility in synthetic pathways. Overall, (3-bromo-5-methoxycarbonyl-phenyl)boronic acid is a versatile building block in organic chemistry, with significant implications in both research and industrial applications.
Formula:C8H8BBrO4
InChI:InChI=1/C8H8BBrO4/c1-14-8(11)5-2-6(9(12)13)4-7(10)3-5/h2-4,12-13H,1H3
SMILES:COC(=O)c1cc(cc(c1)Br)B(O)O
Synonyms:
  • (3-Bromo-5-(methoxycarbonyl)phenyl)boronicacid
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