(1-(tert-Butoxycarbonyl)-6-methoxy-1H-indol-2-yl)boronic acid

• CAT Number: L045063
• CAS Number: 850568-65-9
• Molecular Formula: C14H18BNO5
• Molecular Weight: 291.11
• Purity: ≥95%
• IUPAC Name: [6-methoxy-1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid
• InChI: InChI=1S/C14H18BNO5/c1-14(2,3)21-13(17)16-11-8-10(20-4)6-5-9(11)7-12(16)15(18)19/h5-8,18-19H,1-4H3
• InChIKey: ATIJYIUOXDCYTN-UHFFFAOYSA-N
• SMILES: B(C1=CC2=C(N1C(=O)OC(C)(C)C)C=C(C=C2)OC)(O)O

(1-(tert-Butoxycarbonyl)-6-methoxy-1H-indol-2-yl)boronic acid(CAT: L045063) is a high-purity boronic acid derivative featuring a protected indole core with a tert-butoxycarbonyl (Boc) group and a methoxy substitution. This versatile compound serves as a critical intermediate in pharmaceutical research and organic synthesis, particularly in the development of bioactive molecules, small-molecule inhibitors, and advanced heterocyclic frameworks. The boronic acid functionality allows for efficient cross-coupling reactions, such as Suzuki-Miyaura coupling, enabling the synthesis of complex molecules and therapeutic candidates. (1-(tert-Butoxycarbonyl)-6-methoxy-1H-indol-2-yl)boronic acid is ideal for applications in medicinal chemistry, providing stability, reactivity, and precision for academic and industrial research innovations.