(4-((tert-Butoxycarbonyl)amino)-5-(methoxycarbonyl)thiophen-2-yl)boronic acid

• CAT Number: L021696
• CAS Number: 2377608-25-6
• Molecular Formula: C11H16BNO6S
• Molecular Weight: 301.13
• Purity: ≥95%
• IUPAC Name: [5-methoxycarbonyl-4-[(2-methylpropan-2-yl)oxycarbonylamino]thiophen-2-yl]boronic acid
• InChI: InChI=1S/C11H16BNO6S/c1-11(2,3)19-10(15)13-6-5-7(12(16)17)20-8(6)9(14)18-4/h5,16-17H,1-4H3,(H,13,15)
• InChIKey: IAIBDIUVAWDVBF-UHFFFAOYSA-N
• SMILES: B(C1=CC(=C(S1)C(=O)OC)NC(=O)OC(C)(C)C)(O)O

(4-((tert-Butoxycarbonyl)amino)-5-(methoxycarbonyl)thiophen-2-yl)boronic acid is a boronic acid derivative featuring a thiophene ring substituted with a tert-butoxycarbonyl (Boc) amino group at the 4-position and a methoxycarbonyl (-COOCH₃) group at the 5-position. The boronic acid group offers the compound unique reactivity, particularly in Suzuki coupling reactions for organic synthesis. This compound is useful in the design of complex molecules, especially in medicinal chemistry, where it may be explored for pharmaceutical applications targeting various biological pathways or for materials science.