(4-(((Benzyloxy)carbonyl)(ethyl)amino)phenyl)boronic acid

• CAT Number: L034974
• CAS Number: 1221448-69-6
• Molecular Formula: C16H18BNO4
• Molecular Weight: 299.11
• Purity: ≥95%
• IUPAC Name: [4-[ethyl(phenylmethoxycarbonyl)amino]phenyl]boronic acid
• InChI: InChI=1S/C16H18BNO4/c1-2-18(15-10-8-14(9-11-15)17(20)21)16(19)22-12-13-6-4-3-5-7-13/h3-11,20-21H,2,12H2,1H3
• InChIKey: ZQSANIXVXNVIRM-UHFFFAOYSA-N
• SMILES: B(C1=CC=C(C=C1)N(CC)C(=O)OCC2=CC=CC=C2)(O)O

(4-(((Benzyloxy)carbonyl)(ethyl)amino)phenyl)boronic Acid(CAT: L034974) is a high-purity boronic acid derivative widely utilized in pharmaceutical, chemical, and material science research. Featuring a benzyloxycarbonyl-ethylamino functional group attached to a phenylboronic acid scaffold, this compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions and the synthesis of bioactive molecules. It is frequently employed in medicinal chemistry for the development of therapeutic agents and the exploration of structure-activity relationships. With excellent stability and reactivity, (4-(((Benzyloxy)carbonyl)(ethyl)amino)phenyl)boronic Acid ensures precision and reliability, making it a critical tool for advanced synthetic and research applications.