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CS-W001157 4
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tert-Butyl 2,2-dimethylpiperazine-1-carboxylate

  • CAS No. 674792-07-5

  • Cat. No. CS-W008574
  • Molecule weight214.31
  • Purity≥97%
  • MDL No.MFCD07371652

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

tert-Butyl 2,2-dimethylpiperazine-1-carboxylate|CS-W008574

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General Information

  • CAS No. 674792-07-5
  • Cat. No. CS-W008574
  • Purity ≥97%
  • MDL No. MFCD07371652
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₂₂N₂O₂
  • Molecular Weight 214.31
  • Synonym(s) 1-BOC-2,2-DIMETHYL-PIPERAZINE
  • SMILES O=C(OC(C)(C)C)N1C(C)(C)CNCC1

Description

tert-Butyl 2,2-dimethylpiperazine-1-carboxylate features a sterically hindered piperazine core with a robust tert-butyl ester protecting group, enabling stable incorporation into complex molecular architectures. The dimethyl substitution enhances solubility and reduces basicity, facilitating handling under standard bench conditions. This derivative serves as a key intermediate in medicinal chemistry for constructing bioactive heterocycles.

Application

tert-Butyl 2,2-dimethylpiperazine-1-carboxylate serves as a stable, bench-friendly piperazine scaffold for medicinal chemistry applications. Its tert-butyl carbamate group enables straightforward deprotection under mild acidic conditions, while the 2,2-dimethyl substitution enhances steric shielding and metabolic stability. The compound functions effectively in coupling reactions and facilitates the construction of complex heterocyclic architectures with improved solubility and purification profiles.

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   41.57
  • LogP   1.6053
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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