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CAS 850589-48-9

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[3-chloro-4-(diethylcarbamoyl)phenyl]boronic acid

Description:
[3-Chloro-4-(diethylcarbamoyl)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 applications, including organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring, which can influence its reactivity and solubility. The diethylcarbamoyl group enhances its potential for biological activity, as it may improve the compound's interaction with biological targets. This substance is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its boronic acid functionality allows it to participate in Suzuki-Miyaura cross-coupling reactions, a valuable method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the chlorine atom can provide unique electronic properties, potentially affecting the compound's reactivity and stability. Overall, [3-chloro-4-(diethylcarbamoyl)phenyl]boronic acid is a versatile compound with applications in both synthetic and medicinal chemistry.
Formula:C11H15BClNO3
InChI:InChI=1/C11H15BClNO3/c1-3-14(4-2)11(15)9-6-5-8(12(16)17)7-10(9)13/h5-7,16-17H,3-4H2,1-2H3
SMILES:CCN(CC)C(=O)c1ccc(cc1Cl)B(O)O
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