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CAS 874460-05-6

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

Description:
[4-(2-chloroethylcarbamoyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a 2-chloroethylcarbamoyl group, which enhances its reactivity and potential biological activity. The presence of the chloroethyl moiety may impart specific pharmacological properties, making it of interest in drug development. This compound is typically solid at room temperature and may exhibit solubility in polar organic solvents. Its boronic acid functionality allows it to participate in various coupling reactions, such as Suzuki-Miyaura cross-coupling, which is valuable in the synthesis of complex organic molecules. Additionally, the compound's structural characteristics suggest potential applications in targeted therapies, particularly in cancer treatment, due to the selective nature of boronic acids in biological systems. Safety and handling precautions should be observed, as with all chemical substances, particularly those containing halogens and reactive functional groups.
Formula:C9H11BClNO3
InChI:InChI=1/C9H11BClNO3/c11-5-6-12-9(13)7-1-3-8(4-2-7)10(14)15/h1-4,14-15H,5-6H2,(H,12,13)
SMILES:c1cc(ccc1C(=O)NCCCl)B(O)O
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