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CS-W001157 4
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Piperidine-4-carboxamide

  • CAS No. 39546-32-2

  • Cat. No. CS-W013464
  • Purity≥97%
  • MDL No.MFCD00038012

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

Piperidine-4-carboxamide|CS-W013464

Structure of 39546-32-2

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General Information

  • CAS No. 39546-32-2
  • Cat. No. CS-W013464
  • Purity ≥97%
  • MDL No. MFCD00038012
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₁₂N₂O
  • Molecular Weight 128.17
  • Synonym(s) 4-Piperidinecarboxamide
  • SMILES O=C(N)C1CCNCC1

Description

t-Boc-N-amido-PEG6-acid is a PEG linker containing a terminal carboxylic acid and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Synthesis

  • Route1
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    • ~0%
    • In-stock
      Piperidine-4-carboxamide|CS-W013464
      39546-32-2
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      150479-48-4

    References

    • Pfizer Inc. Patent: US5482941 A1, 1996 ; US 5482941 A
  • Route2
    • Isonicotinamide Isoniazid  Impurity|CS-0229453
      1453-82-3
    • ~%
    • In-stock
      Piperidine-4-carboxamide|CS-W013464
      39546-32-2

    References

    • Cui, Yi; Kwok, Samantha; Bucholtz, Andrew; Davis, Boyd; Whitney, Ralph A.; Jessop, Philip G. New Journal of Chemistry, 2008 , vol. 32, # 6 p. 1027 - 1037
  • Route3

    References

    • Itani, Hiromichi; Ito, Harunobu; Sakata, Yoshihiko; Hatakeyama, Yoshifumi; Oohashi, Hiroko; Satoh, Yoshinari Bioorganic and Medicinal Chemistry Letters, 2002 , vol. 12, # 5 p. 757 - 761

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   55.12
  • LogP   -0.5287
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   1

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