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CS-W001157 4
Total: USD 88.00

tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate

  • CAS No. 170911-92-9

  • Cat. No. CS-W005015
  • Purity≥97%
  • MDL No.MFCD04115065

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

tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate|CS-W005015

Structure of 170911-92-9

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General Information

  • CAS No. 170911-92-9
  • Cat. No. CS-W005015
  • Purity ≥97%
  • MDL No. MFCD04115065
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₂₃N₃O₂
  • Molecular Weight 277.36
  • Synonym(s) 4-(4-Boc-piperazin-1-yl)aniline
  • SMILES C(C)(C)(C)OC(=O)N1CCN(CC1)C2=CC=C(C=C2)N

Description

tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate features a piperazine core linked to a para-aminophenyl group, delivering a robust scaffold for medicinal chemistry. The tert-butyl ester moiety enhances solubility and stability while enabling straightforward deprotection under mild acidic conditions. This compound serves as a key intermediate in the synthesis of bioactive molecules, particularly those targeting CNS disorders and kinase pathways.

Application

tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate serves as a versatile building block for the synthesis of biologically active piperazine-based compounds. Its robust tert-butoxycarbonyl (Boc) group offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The pendant aniline functionality enables direct coupling reactions, including Suzuki-Miyaura, Ullmann, and reductive amination, making it ideal for constructing diverse heterocyclic scaffolds and drug candidates 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   58.8
  • LogP   2.3259
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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