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CS-W001157 4
Total: USD 88.00

Boc-Asp-OH

  • CAS No. 13726-67-5

  • Cat. No. CS-0020432
  • Purity≥97%
  • MDL No.MFCD00037279

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

Boc-Asp-OH|CS-0020432

Structure of 13726-67-5

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General Information

  • CAS No. 13726-67-5
  • Cat. No. CS-0020432
  • Purity ≥97%
  • MDL No. MFCD00037279
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₅NO₆
  • Molecular Weight 233.22
  • Synonym(s) None
  • SMILES O=C(O)[C@H](CC(O)=O)NC(OC(C)(C)C)=O

Description

Boc-Asp-OH serves as a protected aspartic acid derivative for peptide synthesis, featuring a stable tert-butoxycarbonyl group that enables selective coupling under standard conditions. This bench-stable reagent integrates seamlessly into N-terminal protection strategies, offering reliable handling and compatibility with diverse coupling protocols.

Synthesis

  • Route1

    References

    • Deutsches Krebsforschungszentrum Stiftung des oeffentlichen Rechts Patent: EP1647283 A1, 2006 ; Location in patent: Page/Page column 5 ;
  • Route2

    References

    • Channe Gowda Tetrahedron Letters, 2002 , vol. 43, # 2 p. 311 - 313
  • Route3
    • In-stock
      L-Aspartic acid|CS-0009701
      56-84-8
    • null|null
      98015-52-2
    • ~61%
    • In-stock
      Boc-Asp-OH|CS-0020432
      13726-67-5

    References

    • Societe Nationale des Poudres et Explosifs Patent: US4725680 A1, 1988 ;

Safety Information

Download SDS
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

Quality Control

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Computational Chemistry Data

  • TPSA   112.93
  • LogP   0.439
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   4

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