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CAS 874288-30-9

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[3-[(2-bromophenyl)carbamoyl]phenyl]boronic acid

Description:
[3-[(2-bromophenyl)carbamoyl]phenyl]boronic acid, with the CAS number 874288-30-9, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a carbamoyl substituent. 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 bromophenyl group may impart additional reactivity and influence its solubility and stability in different solvents. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Furthermore, the compound may exhibit biological activity, potentially serving as a pharmacophore in drug development. Its structural features suggest it could interact with biological targets, making it of interest in the field of medicinal chemistry. Overall, this compound represents a versatile building block in synthetic organic chemistry and has potential applications in pharmaceuticals and materials science.
Formula:C13H11BBrNO3
InChI:InChI=1/C13H11BBrNO3/c15-11-6-1-2-7-12(11)16-13(17)9-4-3-5-10(8-9)14(18)19/h1-8,18-19H,(H,16,17)
SMILES:c1ccc(c(c1)Br)N=C(c1cccc(c1)B(O)O)O
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