(3-((tert-Butoxycarbonyl)amino)-4-chlorophenyl)boronic acid

• CAT Number: L032582
• CAS Number: 871329-57-6
• Molecular Formula: C11H15BClNO4
• Molecular Weight: 271.51
• Purity: ≥95%
• IUPAC Name: [4-chloro-3-[(2-methylpropan-2-yl)oxycarbonylamino]phenyl]boronic acid
• InChI: InChI=1S/C11H15BClNO4/c1-11(2,3)18-10(15)14-9-6-7(12(16)17)4-5-8(9)13/h4-6,16-17H,1-3H3,(H,14,15)
• InChIKey: YDGKXXRWQFCXOO-UHFFFAOYSA-N
• SMILES: B(C1=CC(=C(C=C1)Cl)NC(=O)OC(C)(C)C)(O)O

(3-((tert-Butoxycarbonyl)amino)-4-chlorophenyl)boronic acid is an organic compound featuring a boronic acid group attached to a chlorophenyl ring, with a tert-butoxycarbonyl (Boc) protected amino group at the third position. Its chemical formula is C₁₁H₁₄BClN₁O₃. This compound is significant in organic synthesis, particularly in coupling reactions due to the reactivity of the boronic acid moiety. The Boc protection allows for selective deprotection, making it a valuable intermediate in the synthesis of pharmaceuticals and other bioactive compounds.