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tert-Butyl (1-(2-aminoethyl)piperidin-4-yl)carbamate

  • CAS No. 259180-79-5

  • Cat. No. CS-0127719
  • Purity≥97%
  • MDL No.MFCD18373985

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

tert-Butyl (1-(2-aminoethyl)piperidin-4-yl)carbamate|CS-0127719

Structure of 259180-79-5

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General Information

  • CAS No. 259180-79-5
  • Cat. No. CS-0127719
  • Purity ≥97%
  • MDL No. MFCD18373985
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₂₅N₃O₂
  • Molecular Weight 243.35
  • Synonym(s) None
  • SMILES O=C(OC(C)(C)C)NC1CCN(CCN)CC1

Description

This tert-butyl (1-(2-aminoethyl)piperidin-4-yl)carbamate features a piperidine core functionalized with a primary amine and a robust tert-butyloxycarbonyl protecting group. The pendant aminoethyl side chain enables facile conjugation or further derivatization, while the carbamate moiety ensures stability during synthesis and storage. This compound serves as a key intermediate in the construction of bioactive molecules, particularly in medicinal chemistry campaigns targeting CNS therapeutics.

Application

tert-Butyl (1-(2-aminoethyl)piperidin-4-yl)carbamate serves as a versatile bifunctional building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. The pendant primary amine facilitates conjugation and derivatization, while the tert-butoxycarbonyl (Boc) group provides orthogonal protection for nitrogen functionalization. Its stability under standard synthetic conditions and ease of deprotection make it ideal for multi-step synthesis and peptide-coupling 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-H319
Precautionary Statements : P264-P270-P280-P330-P501

Quality Control

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Computational Chemistry Data

  • TPSA   67.59
  • LogP   0.9342
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   3

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