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CAS 850567-41-8

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[4-(3-bromopropylcarbamoyl)phenyl]boronic acid

Description:
[4-(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. This compound features a phenyl ring substituted with a carbamoyl group and a bromopropyl chain, contributing to its potential reactivity and solubility properties. The bromine atom can serve as a site for nucleophilic substitution reactions, while the boronic acid moiety can participate in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The compound's structure suggests it may exhibit moderate polarity, influencing its solubility in various organic solvents and water. Additionally, the presence of the boronic acid group allows for potential applications in drug development, particularly in the design of inhibitors or as intermediates in the synthesis of more complex molecules. Overall, [4-(3-bromopropylcarbamoyl)phenyl]boronic acid is a versatile compound with significant implications in chemical research and development.
Formula:C10H13BBrNO3
InChI:InChI=1/C10H13BBrNO3/c12-6-1-7-13-10(14)8-2-4-9(5-3-8)11(15)16/h2-5,15-16H,1,6-7H2,(H,13,14)
SMILES:C(CBr)CNC(=O)c1ccc(cc1)B(O)O
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