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CS-W001157 4
Total: USD 88.00

Fmoc-Asp-OMe

  • CAS No. 145038-52-4

  • Cat. No. CS-W022722
  • Purity≥97%
  • MDL No.MFCD03701473

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

Fmoc-Asp-OMe|CS-W022722

Structure of 145038-52-4

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General Information

  • CAS No. 145038-52-4
  • Cat. No. CS-W022722
  • Purity ≥97%
  • MDL No. MFCD03701473
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₀H₁₉NO₆
  • Molecular Weight 369.37
  • Synonym(s) None
  • SMILES O=C(O)C[C@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)C(OC)=O

Description

Fmoc-Asp-OMe features a protected aspartic acid residue with orthogonal functionality for peptide synthesis. The Fmoc group enables base-labile N-terminal deprotection, while the methyl ester stabilizes the C-terminal carboxylate. This combination facilitates efficient coupling and selective modification in solid-phase workflows, offering reliable handling and compatibility with standard protocols.

Application

Fmoc-Asp-OMe serves as a key building block in solid-phase peptide synthesis, offering orthogonal protection for both the α-amino and side-chain carboxyl groups. The Fmoc group enables efficient base-labile deprotection, while the methyl ester prevents unwanted side reactions during coupling. Its bench-stable nature and compatibility with standard coupling reagents facilitate reliable incorporation into peptide sequences, particularly in the synthesis of acidic or complex peptide scaffolds.

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   101.93
  • LogP   2.5414
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   6

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