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CS-W001157 4
Total: USD 88.00

4-Amino-1-(1-Boc-piperidin-4-yl)-1H-pyrazole

  • CAS No. 1029413-55-5

  • Cat. No. CS-W003734
  • Purity≥96%
  • MDL No.MFCD10687120

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

4-Amino-1-(1-Boc-piperidin-4-yl)-1H-pyrazole|CS-W003734

Structure of 1029413-55-5

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General Information

  • CAS No. 1029413-55-5
  • Cat. No. CS-W003734
  • Purity ≥96%
  • MDL No. MFCD10687120
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₂₂N₄O₂
  • Molecular Weight 266.34
  • Synonym(s) Tert-butyl 4-(4-amino-1h-pyrazol-1-yl)piperidine-1-carboxylate
  • SMILES CC(C)(OC(N1CCC(N2C=C(N)C=N2)CC1)=O)C

Description

4-Amino-1-(1-Boc-piperidin-4-yl)-1H-pyrazole features a Boc-protected piperidine moiety linked to a pyrazole core, delivering a stable, moisture-tolerant scaffold for medicinal chemistry. The electron-rich pyrazole ring pairs with the primary amine to enable direct coupling in peptide and small-molecule synthesis. This derivative integrates readily into diverse heterocyclic frameworks under standard conditions.

Application

4-Amino-1-(1-Boc-piperidin-4-yl)-1H-pyrazole serves as a versatile building block in medicinal chemistry, enabling the construction of complex heterocyclic scaffolds. The Boc-protected piperidine moiety offers excellent bench stability and compatibility with standard deprotection protocols, while the pyrazole core provides a robust platform for further functionalization. Its amine functionality facilitates conjugation reactions and enables access to diverse analogs through common coupling strategies. This compound functions effectively in multi-step syntheses requiring orthogonality and predictable reactivity.

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   73.38
  • LogP   2.0373
  • H_Acceptors   5
  • H_Donors   1
  • Rotatable_Bonds   1

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