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CAS 850567-33-8

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[3-(2-methoxyethylcarbamoyl)phenyl]boronic acid

Description:
[3-(2-Methoxyethylcarbamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a carbamoyl group, specifically a 2-methoxyethyl group, enhancing its solubility and reactivity. The boronic acid moiety contributes to its potential applications in medicinal chemistry, particularly in drug development and as a building block in organic synthesis. The compound is likely to exhibit moderate polarity due to the presence of both hydrophobic (phenyl) and hydrophilic (carbamoyl and methoxyethyl) groups, influencing its interactions in biological systems. Additionally, it may participate in various chemical reactions, including Suzuki coupling, which is significant in the formation of carbon-carbon bonds. Its unique structure and functional groups suggest potential utility in targeted therapies or as a tool in chemical biology, although specific applications would depend on further research and characterization.
Formula:C10H14BNO4
InChI:InChI=1/C10H14BNO4/c1-16-6-5-12-10(13)8-3-2-4-9(7-8)11(14)15/h2-4,7,14-15H,5-6H2,1H3,(H,12,13)
SMILES:COCCN=C(c1cccc(c1)B(O)O)O
Synonyms:
  • {3-[(2-Methoxyethyl)carbamoyl]phenyl}boronic acid
  • boronic acid, B-[3-[[(2-methoxyethyl)amino]carbonyl]phenyl]-
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