(4-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl)boronic acid

• CAT Number: L037444
• CAS Number: 957034-29-6
• Molecular Formula: C13H15BBrNO4
• Molecular Weight: 339.98
• Purity: ≥95%
• IUPAC Name: [4-bromo-1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid
• InChI: InChI=1S/C13H15BBrNO4/c1-13(2,3)20-12(17)16-10-6-4-5-9(15)8(10)7-11(16)14(18)19/h4-7,18-19H,1-3H3
• InChIKey: WWSBCMYHAIKIPV-UHFFFAOYSA-N

(4-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl)boronic acid(CAT: L037444) is a boronic acid derivative of indole, featuring a bromine atom at the 4-position and a tert-butoxycarbonyl (Boc) protecting group on the nitrogen. This compound is particularly valuable in medicinal chemistry and organic synthesis due to its dual functionalization, which allows for selective reactions in complex molecule construction. The boronic acid group is highly versatile, enabling Suzuki-Miyaura cross-coupling reactions that facilitate the attachment of various aromatic and heteroaromatic groups. The Boc-protecting group offers stability during synthesis, making this compound ideal for designing novel indole-based scaffolds in drug discovery, such as kinase inhibitors or anticancer agents. Its reactivity and stability make it a critical tool for researchers focused on developing advanced pharmaceutical and material science applications.