3-(4-Cyanophenyl)aminocarbonylphenylboronic acid

• CAT Number: L032591
• CAS Number: 850567-36-1
• Molecular Formula: C14H11BN2O3
• Molecular Weight: 266.06
• Purity: ≥95%
• IUPAC Name: [3-[(4-cyanophenyl)carbamoyl]phenyl]boronic acid
• InChI: InChI=1S/C14H11BN2O3/c16-9-10-4-6-13(7-5-10)17-14(18)11-2-1-3-12(8-11)15(19)20/h1-8,19-20H,(H,17,18)
• InChIKey: WDWVOWXKMQNJOX-UHFFFAOYSA-N
• SMILES: B(C1=CC(=CC=C1)C(=O)NC2=CC=C(C=C2)C#N)(O)O

3-(4-Cyanophenyl)aminocarbonylphenylboronic acid(CAT: L032591) is a boronic acid derivative featuring a cyanophenyl-substituted carbamoyl group and a boronic acid moiety. This compound is widely utilized in pharmaceutical and chemical research as a versatile intermediate for the synthesis of biologically active molecules, including enzyme inhibitors and receptor modulators. Its boronic acid functionality enables applications in Suzuki-Miyaura coupling reactions, facilitating the development of complex organic structures. With high purity and excellent stability, 3-(4-Cyanophenyl)aminocarbonylphenylboronic acid is a valuable building block for medicinal chemistry, drug discovery, and advanced synthetic applications.