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CAS 850567-42-9

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[3-(3-bromopropylcarbamoyl)phenyl]boronic acid

Description:
[3-(3-bromopropylcarbamoyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a 3-bromopropylcarbamoyl group, which introduces both a bromine atom and a carbamoyl moiety, enhancing its reactivity and potential biological activity. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the bromopropyl chain may contribute to the compound's solubility and interaction with biological targets. Overall, this compound's unique structure and functional groups suggest potential applications in drug development and materials science, particularly in the design of targeted therapies and advanced materials.
Formula:C10H13BBrNO3
InChI:InChI=1/C10H13BBrNO3/c12-5-2-6-13-10(14)8-3-1-4-9(7-8)11(15)16/h1,3-4,7,15-16H,2,5-6H2,(H,13,14)
SMILES:c1cc(cc(c1)B(O)O)C(=NCCCBr)O
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