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CS-W001157 4
Total: USD 88.00

1-Boc-3-Ethyl-piperidin-4-one

  • CAS No. 117565-57-8

  • Cat. No. CS-0061469
  • Purity≥96%
  • MDL No.None

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

1-Boc-3-Ethyl-piperidin-4-one|CS-0061469

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General Information

  • CAS No. 117565-57-8
  • Cat. No. CS-0061469
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₂₁NO₃
  • Molecular Weight 227.30
  • Synonym(s) 1-BOC-3-ETHYL-PIPERIDIN-4-ONE
  • SMILES CCC1CN(CCC1=O)C(=O)OC(C)(C)C

Description

tert-Butyl 3-ethyl-4-oxopiperidine-1-carboxylate features a sterically hindered piperidinone core with a bench-stable carbamate protecting group. This compound integrates readily into synthetic sequences requiring selective nitrogen functionalization, offering enhanced solubility and stability under standard conditions.

Application

tert-Butyl 3-ethyl-4-oxopiperidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. The ketone functionality at C4 supports selective reduction, enolate formation, and nucleophilic addition, while the tert-butoxycarbonyl (Boc) group provides stable protection for nitrogen during multistep synthesis. Its bench-stable nature and compatibility with standard coupling and functionalization protocols facilitate straightforward purification and integration into complex molecular architectures.

Synthesis

  • Route1
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      79099-07-3
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      75-03-6
    • ~%
    • In-stock
      1-Boc-3-Ethyl-piperidin-4-one|CS-0061469
      117565-57-8

    References

    • Luly, Jay R.; Nakasato, Yoshisuke; Ohshima, Etsuo; Harriman, Geraldine C.B.; Carson, Kenneth G.; Ghosh, Shomir; Elder, Amy M.; Mattia, Karen M. Patent: US2005/70549 A1, 2005 ;

Safety Information

Download SDS
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   46.61
  • LogP   2.2225
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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