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CS-W001157 4
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(R)-1-Boc-2-Hydroxymethyl-piperazine

  • CAS No. 169448-87-7

  • Cat. No. CS-D0658
  • Purity≥95%
  • MDL No.MFCD07772092

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

(R)-1-Boc-2-Hydroxymethyl-piperazine|CS-D0658

Structure of 169448-87-7

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General Information

  • CAS No. 169448-87-7
  • Cat. No. CS-D0658
  • Purity ≥95%
  • MDL No. MFCD07772092
  • Storage RT, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₂₀N₂O₃
  • Molecular Weight 216.28
  • Synonym(s) tert-butyl (2R)-2-(hydroxymethyl)piperazine-1-carboxylate
  • SMILES O=C(OC(C)(C)C)N1[C@@H](CO)CNCC1

Description

(R)-1-Boc-2-Hydroxymethyl-piperazine features a chiral piperazine core with a stable Boc-protected amine and a pendant hydroxymethyl group, enabling selective derivatization. This bench-stable scaffold integrates readily into complex molecular architectures, offering enhanced solubility and functional handle versatility in medicinal chemistry workflows.

Application

(R)-1-Boc-2-hydroxymethylpiperazine serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient access to piperazine-based scaffolds. The Boc group provides stable protection of the primary amine, while the pendant hydroxymethyl functionality allows for further derivatization via oxidation or coupling reactions. Its bench-stable nature and compatibility with standard peptide and heterocyclic coupling protocols make it well-suited for medicinal chemistry and process development workflows.

Synthesis

  • Route1

    References

    • ASTRAZENECA AB; ASTRAZENECA UK LIMITED Patent: WO2005/26152 A1, 2005 ; Location in patent: Page/Page column 136 ; WO 2005/026152 A1

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   61.8
  • LogP   0.1876
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   1

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