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tert-butyl (S)-2-(methoxymethyl)piperazine-1-carboxylate

  • CAS No. 1217728-72-7

  • Cat. No. CS-0030320
  • Purity≥95%
  • MDL No.MFCD11112289

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

tert-butyl (S)-2-(methoxymethyl)piperazine-1-carboxylate|CS-0030320

Structure of 1217728-72-7

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General Information

  • CAS No. 1217728-72-7
  • Cat. No. CS-0030320
  • Purity ≥95%
  • MDL No. MFCD11112289
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₂₂N₂O₃
  • Molecular Weight None
  • Synonym(s) tert-butyl (2S)-2-(methoxymethyl)piperazine-1-carboxylate
  • SMILES O=C(N1[C@H](COC)CNCC1)OC(C)(C)C

Description

This tert-butyl (S)-2-(methoxymethyl)piperazine-1-carboxylate features a chiral piperazine core with a methoxymethyl group at the 2-position and a tert-butyloxycarbonyl protecting group. The molecule combines enhanced solubility with stability under standard bench conditions, enabling efficient incorporation into complex molecular architectures. Its defined stereochemistry supports precise synthetic pathways in medicinal chemistry applications.

Application

tert-butyl (S)-2-(methoxymethyl)piperazine-1-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of piperazine-based scaffolds with defined stereochemistry. The tert-butyl carbamate group provides excellent stability and ease of removal under mild acidic conditions, while the methoxymethyl side chain offers orthogonal functionalization potential. This compound facilitates efficient access to bioactive molecules through standard coupling and derivatization protocols, making it well-suited for high-throughput library synthesis and API development.

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   50.8
  • LogP   0.8417
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   2

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