1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperidine

• CAT Number: L020334
• CAS Number: 852227-96-4
• Molecular Formula: C17H26BNO2
• Molecular Weight: 287.2
• Purity: ≥95%
• Storage: 2-8°C
• IUPAC Name: 1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperidine
• InChI: InChI=1S/C17H26BNO2/c1-16(2)17(3,4)21-18(20-16)14-8-10-15(11-9-14)19-12-6-5-7-13-19/h8-11H,5-7,12-13H2,1-4H3
• InChIKey: OTOKWHGMHAAFRM-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)N3CCCCC3

1-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperidine (Cat No.:L020334) is a chemical compound with a piperidine ring substituted by a phenyl group at the 1-position. The phenyl group contains a 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) substituent, which is a boronate ester. This versatile compound serves as an essential building block in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. The boronate ester functionality allows coupling with various electrophiles, enabling the creation of diverse molecules with potential applications in drug development or research.