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CAS 850593-04-3

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[4-(2-hydroxyethylcarbamoyl)phenyl]boronic acid

Description:
[4-(2-hydroxyethylcarbamoyl)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 that is further modified by a hydroxyethyl moiety, enhancing its solubility and reactivity. The boronic acid functionality allows it to participate in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Its structural attributes contribute to its potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the presence of the hydroxyethyl group may influence its interaction with biological systems, potentially enhancing its pharmacological properties. The compound is typically handled with standard laboratory safety precautions, as with other boronic acids, due to its reactivity and potential environmental impact. Overall, [4-(2-hydroxyethylcarbamoyl)phenyl]boronic acid represents a versatile building block in the synthesis of complex organic molecules.
Formula:C9H12BNO4
InChI:InChI=1/C9H12BNO4/c12-6-5-11-9(13)7-1-3-8(4-2-7)10(14)15/h1-4,12,14-15H,5-6H2,(H,11,13)
SMILES:c1cc(ccc1C(=O)NCCO)B(O)O
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