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1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine

  • CAS No. 1264198-72-2

  • Cat. No. CS-0120400
  • Molecule weight225.14
  • Purity≥98%
  • MDL No.MFCD11506064

*For research and further manufacturing use only, not for direct human use.

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine|CS-0120400

Structure of 1264198-72-2

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General Information

  • CAS No. 1264198-72-2
  • Cat. No. CS-0120400
  • Purity ≥98%
  • MDL No. MFCD11506064
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₂₄BNO₂
  • Molecular Weight 225.14
  • Synonym(s) 1-Methyl-piperidine-4-boronic acid pinacol ester
  • SMILES CN1CCC(B2OC(C)(C)C(C)(C)O2)CC1

Description

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine features a stable boronate ester group enabling efficient Suzuki-Miyaura coupling. The piperidine core provides a versatile nitrogen handle for medicinal chemistry applications. Bench-stable under standard conditions, this reagent integrates seamlessly into iterative synthesis workflows.

Application

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its tetramethylboronate group enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and compatibility in late-stage diversification of heterocyclic scaffolds. The piperidine core provides a valuable nitrogen-containing motif for medicinal chemistry applications, while the protected boron moiety ensures high stability and ease of purification.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   21.7
  • LogP   2.1744
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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