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CS-W001157 4
Total: USD 88.00

Boc-Pip-OH

  • CAS No. 26250-84-0

  • Cat. No. CS-W007743
  • Purity≥97%
  • MDL No.MFCD00151904

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

Boc-Pip-OH|CS-W007743

Structure of 26250-84-0

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General Information

  • CAS No. 26250-84-0
  • Cat. No. CS-W007743
  • Purity ≥97%
  • MDL No. MFCD00151904
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₉NO₄
  • Molecular Weight 229.28
  • Synonym(s) Boc-L-pipecolic acid
  • SMILES [C@@H]1(N(C(OC(C)(C)C)=O)CCCC1)C(=O)O

Description

Boc-Pip-OH is a bench-stable, moisture-tolerant amino acid derivative featuring a tert-butoxycarbonyl-protected primary amine and a terminal hydroxyl group. This combination enables straightforward coupling reactions in peptide synthesis workflows, where the Boc group facilitates selective deprotection and the hydroxyl moiety supports derivatization or conjugation.

Synthesis

  • Route1
    • 1-(Tert-butoxycarbonyl)-1,4,5,6-tetrahydropyridine-2-carboxylic acid|CS-0661058
      259133-67-0
    • ~87%
    • In-stock
      Boc-Pip-OH|CS-W007743
      26250-84-0

    References

    • Wilkinson; Stehle; Beak Organic letters, 2000 , vol. 2, # 2 p. 155 - 158
  • Route2
    • null|null
      7681-38-1
    • null|null
      13406-98-9
    • In-stock
      Di-tert-butyl dicarbonate|CS-0017817
      24424-99-5
    • ~72%
    • In-stock
      Boc-Pip-OH|CS-W007743
      26250-84-0

    References

    • Agouron Pharmaceuticals, Inc. Patent: US5484926 A1, 1996 ;
  • Route3

    References

    • Thai, Dung L.; Sapko, Michael T.; Reiter, Clara T.; Bierer, Donald E.; Perel, James M. Journal of Medicinal Chemistry, 1998 , vol. 41, # 4 p. 591 - 601

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-P304+P340-P362-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   66.84
  • LogP   1.8606
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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