(3-Chloro-4-(chlorocarbonyl)phenyl)boronic acid

• CAT Number: L035027
• CAS Number: 850589-38-7
• Molecular Formula: C7H5BCl2O3
• Molecular Weight: 218.83
• Purity: ≥95%
• IUPAC Name: (4-carbonochloridoyl-3-chlorophenyl)boronic acid
• InChI: InChI=1S/C7H5BCl2O3/c9-6-3-4(8(12)13)1-2-5(6)7(10)11/h1-3,12-13H
• InChIKey: OYBLIGPPYFOHAZ-UHFFFAOYSA-N
• SMILES: B(C1=CC(=C(C=C1)C(=O)Cl)Cl)(O)O

(3-Chloro-4-(chlorocarbonyl)phenyl)boronic Acid(CAT: L035027) is a high-purity boronic acid derivative widely employed in pharmaceutical, chemical, and material science research. Featuring a chlorinated aromatic ring with boronic acid and chlorocarbonyl functional groups, this compound is a versatile intermediate for Suzuki-Miyaura cross-coupling reactions and the synthesis of complex organic molecules. It is particularly valuable in medicinal chemistry for developing bioactive compounds and exploring structure-activity relationships. With excellent stability and reactivity, (3-Chloro-4-(chlorocarbonyl)phenyl)boronic Acid ensures precision and reliability, making it an essential tool for advanced research and innovative synthetic applications.