(4-((tert-Butoxycarbonyl)amino)-2-fluorophenyl)boronic acid

• CAT Number: L026603
• CAS Number: 1415960-56-3
• Molecular Formula: C11H15BFNO4
• Molecular Weight: 255.05
• Purity: ≥95%
• IUPAC Name: [2-fluoro-4-[(2-methylpropan-2-yl)oxycarbonylamino]phenyl]boronic acid
• InChI: InChI=1S/C11H15BFNO4/c1-11(2,3)18-10(15)14-7-4-5-8(12(16)17)9(13)6-7/h4-6,16-17H,1-3H3,(H,14,15)
• InChIKey: DAISURXDKVZMGH-UHFFFAOYSA-N
• SMILES: B(C1=C(C=C(C=C1)NC(=O)OC(C)(C)C)F)(O)O

(4-((tert-Butoxycarbonyl)amino)-2-fluorophenyl)boronic acid(CAT: L026603) is a high-purity boronic acid compound widely utilized in pharmaceutical and chemical research. Featuring a fluorinated phenyl ring with a boronic acid functional group, an amino group protected by a tert-butoxycarbonyl (Boc) group, this compound is an essential intermediate for Suzuki-Miyaura cross-coupling reactions. It is particularly valuable in medicinal chemistry for synthesizing complex bioactive molecules and drug candidates. (4-((tert-Butoxycarbonyl)amino)-2-fluorophenyl)boronic acid ensures consistent performance and reliability, supporting advanced research in drug discovery, fine chemical synthesis, and material science.