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CAS 874460-03-4

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

Description:
[4-(3-Chloropropylcarbamoyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a 3-chloropropylcarbamoyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and medicinal chemistry. The presence of the chloropropyl group may enhance its reactivity and solubility in organic solvents. Additionally, the boronic acid moiety can participate in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. The compound's structure suggests potential biological activity, possibly as a pharmaceutical agent, due to the presence of the carbamoyl group, which can influence interactions with biological targets. Overall, [4-(3-chloropropylcarbamoyl)phenyl]boronic acid is a versatile compound with applications in both synthetic and medicinal chemistry.
Formula:C10H13BClNO3
InChI:InChI=1/C10H13BClNO3/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(CCl)CNC(=O)c1ccc(cc1)B(O)O
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