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CS-W001157 4
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(S)-tert-butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate

  • CAS No. 389889-82-1

  • Cat. No. CS-M2972
  • Purity≥98%
  • MDL No.MFCD22666103

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

(S)-tert-butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate|CS-M2972

Structure of 389889-82-1

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General Information

  • CAS No. 389889-82-1
  • Cat. No. CS-M2972
  • Purity ≥98%
  • MDL No. MFCD22666103
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₂₃NO₃
  • Molecular Weight 229.32
  • Synonym(s) tert-butyl 4-[(1S)-1-hydroxyethyl]piperidine-1-carboxylate
  • SMILES O=C(OC(C)(C)C)N1CCC(CC1)[C@H](C)O

Description

(S)-tert-butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate features a chiral piperidine core with a pendant hydroxyl-bearing ethyl group, enabling direct functionalization at the alcohol site. This bench-stable, moisture-tolerant building block integrates seamlessly into asymmetric synthesis workflows, delivering high enantiomeric purity for complex molecule construction.

Application

(S)-tert-Butyl 4-(1-hydroxyethyl)piperidine-1-carboxylate serves as a chiral building block for piperidine-based pharmaceutical intermediates. The pendant hydroxyl group enables direct functionalization via oxidation or derivatization, while the tert-butoxycarbonyl (Boc) group provides stable protection under standard conditions. Its bench-stable, crystalline nature facilitates handling and purification, supporting scalable synthesis in medicinal chemistry workflows.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   49.77
  • LogP   2.0143
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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