(1-(tert-Butoxycarbonyl)-1H-indol-4-yl)boronic acid

• CAT Number: L029301
• CAS Number: 2102451-30-7
• Molecular Formula: C13H16BNO4
• Molecular Weight: 261.08
• Purity: ≥95%
• IUPAC Name: [1-[(2-methylpropan-2-yl)oxycarbonyl]indol-4-yl]boronic acid
• InChI: InChI=1S/C13H16BNO4/c1-13(2,3)19-12(16)15-8-7-9-10(14(17)18)5-4-6-11(9)15/h4-8,17-18H,1-3H3
• InChIKey: JFCFJRCULIWLNL-UHFFFAOYSA-N
• SMILES: B(C1=C2C=CN(C2=CC=C1)C(=O)OC(C)(C)C)(O)O

(1-(tert-Butoxycarbonyl)-1H-indol-4-yl)boronic acid(CAT: L029301) is a specialized boronic acid derivative widely utilized in organic synthesis and medicinal chemistry. Combining an indole core with a boronic acid functionality and a tert-butoxycarbonyl (Boc) protecting group, this compound serves as a versatile intermediate for constructing complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of diverse bioactive compounds and pharmaceutical candidates. With high purity and consistent performance, (1-(tert-Butoxycarbonyl)-1H-indol-4-yl)boronic acid supports advanced research in drug discovery, material science, and synthetic methodologies. Its functional versatility makes it an indispensable tool for innovative chemical transformations.