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CS-W001157 4
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Tert-butyl 4-(piperidin-4-ylmethyl)piperidine-1-carboxylate

  • CAS No. 879883-54-2

  • Cat. No. CS-0272822
  • Purity≥95%
  • MDL No.MFCD15474945

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

Tert-butyl 4-(piperidin-4-ylmethyl)piperidine-1-carboxylate|CS-0272822

Structure of 879883-54-2

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General Information

  • CAS No. 879883-54-2
  • Cat. No. CS-0272822
  • Purity ≥95%
  • MDL No. MFCD15474945
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₃₀N₂O₂
  • Molecular Weight 282.43
  • Synonym(s) 4-Piperidin-4-ylmethyl-piperidine-1-carboxylic acid tert-butyl ester
  • SMILES O=C(OC(C)(C)C)N1CCC(CC1)CC2CCNCC2

Description

Tert-butyl 4-(piperidin-4-ylmethyl)piperidine-1-carboxylate is a bench-stable, moisture-tolerant piperidine derivative featuring a protected amine and a flexible alkyl linker. This bifunctional scaffold integrates a tertiary amine and a pendant piperidine ring, enabling direct incorporation into complex heterocyclic architectures. It serves as a key intermediate in the synthesis of bioactive molecules requiring spatially defined nitrogen-rich motifs.

Application

Tert-butyl 4-(piperidin-4-ylmethyl)piperidine-1-carboxylate serves as a versatile bis-piperidine building block for medicinal chemistry and target-oriented synthesis. Its tert-butyl carbamate group enables straightforward deprotection under mild acidic conditions, while the piperidin-4-ylmethyl moiety provides a rigidified, amine-functionalized scaffold ideal for constructing complex nitrogen-containing heterocycles. The molecule exhibits excellent bench stability and facilitates efficient functionalization in multistep sequences, making it well-suited for high-throughput library synthesis and API precursor development.

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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

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Computational Chemistry Data

  • TPSA   41.57
  • LogP   3.0232
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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