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CS-W001157 4
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(S)-tert-Butyl 2-(tert-butyl)piperazine-1-carboxylate hydrochloride

  • CAS No. 1381959-73-4

  • Cat. No. CS-0154949
  • Purity≥97%
  • MDL No.MFCD18206293

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

(S)-tert-Butyl 2-(tert-butyl)piperazine-1-carboxylate hydrochloride|CS-0154949

Structure of 1381959-73-4

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General Information

  • CAS No. 1381959-73-4
  • Cat. No. CS-0154949
  • Purity ≥97%
  • MDL No. MFCD18206293
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₂₇ClN₂O₂
  • Molecular Weight 278.82
  • Synonym(s) (S)-tert-butyl 2-tert-butylpiperazine-1-carboxylate hydrochloride
  • SMILES CC(C)([C@H]1CNCCN1C(OC(C)(C)C)=O)C.Cl

Description

This bench-stable, moisture-tolerant piperazine derivative features a tert-butyl-protected amine and a hydrochloride salt form, enabling straightforward incorporation into synthetic sequences. The sterically hindered backbone resists undesired side reactions, while the carboxylate moiety facilitates efficient deprotection under standard conditions.

Application

(S)-tert-Butyl 2-(tert-butyl)piperazine-1-carboxylate hydrochloride serves as a chiral piperazine building block with enhanced stability and ease of handling. Its tert-butyl protecting groups offer robustness under standard synthetic conditions, enabling selective deprotection and functionalization. The molecule facilitates efficient access to pharmaceutically relevant scaffolds through amine coupling, reductive amination, and metal-catalyzed transformations, making it a practical choice for medicinal chemistry campaigns requiring stereocontrol and scalable synthesis.

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   41.57
  • LogP   2.6632
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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