1-Boc-pyrrolidine-3-boronic acid pinacol ester

• CAT Number: M031967
• CAS Number: 1312712-22-3
• Molecular Formula: C15H28BNO4
• Molecular Weight: 297.20
• Purity: ≥95%
• Storage: -20°C
• IUPAC Name: tert-butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrolidine-1-carboxylate
• InChI: InChI=1S/C15H28BNO4/c1-13(2,3)19-12(18)17-9-8-11(10-17)16-20-14(4,5)15(6,7)21-16/h11H,8-10H2,1-7H3
• InChIKey: YADHEMOTVPFRIU-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2CCN(C2)C(=O)OC(C)(C)C

1-Boc-pyrrolidine-3-boronic acid pinacol ester(CAT: M031967) is a valuable reagent in medicinal chemistry and organic synthesis, known for its applications in developing drug candidates and complex organic molecules. The Boc (tert-butoxycarbonyl) group provides protective functionality, preserving the pyrrolidine nitrogen during reactions. The boronic acid pinacol ester moiety enables its use in Suzuki-Miyaura coupling reactions, facilitating the formation of carbon-carbon bonds. This compound is particularly advantageous in synthesizing heterocyclic structures and is widely applied in the design of pharmaceuticals, agrochemicals, and material sciences. Its stability and reactivity make it an indispensable tool for chemists focused on high-precision synthesis.