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CS-W001157 4
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1-tert-Butyl 2-ethyl (2S)-4-oxopiperidine-1,2-dicarboxylate

  • CAS No. 180854-44-8

  • Cat. No. CS-0052402
  • Purity≥97%
  • MDL No.None

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

1-tert-Butyl 2-ethyl (2S)-4-oxopiperidine-1,2-dicarboxylate|CS-0052402

Structure of 180854-44-8

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General Information

  • CAS No. 180854-44-8
  • Cat. No. CS-0052402
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₂₁NO₅
  • Molecular Weight 271.31
  • Synonym(s) (S)-1-tert-Butyl 2-ethyl 4-oxopiperidine-1,2-dicarboxylate
  • SMILES CCOC(=O)[C@@H]1CC(=O)CCN1C(=O)OC(C)(C)C

Description

This chiral piperidine derivative features a bench-stable, moisture-tolerant scaffold with defined stereochemistry at the 2-position. The tert-butyl and ethyl ester groups enable straightforward functionalization, while the 4-oxo moiety provides a reactive handle for downstream transformations in medicinal chemistry applications.

Application

1-tert-Butyl 2-ethyl (2S)-4-oxopiperidine-1,2-dicarboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective synthesis of piperidine-based scaffolds. The protected amine and ester functionalities offer orthogonal reactivity, facilitating downstream transformations such as reductive amination, nucleophilic substitution, and ring functionalization. Bench-stable and readily purified by chromatography, it functions effectively in multi-step sequences for medicinal chemistry and natural product synthesis.

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   72.91
  • LogP   1.5181
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   2

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