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CS-W001157 4
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Boc-D-Asp-OMe

  • CAS No. 137130-65-5

  • Cat. No. CS-0154574
  • Purity≥97%
  • MDL No.MFCD03094776

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

Boc-D-Asp-OMe|CS-0154574

Structure of 137130-65-5

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General Information

  • CAS No. 137130-65-5
  • Cat. No. CS-0154574
  • Purity ≥97%
  • MDL No. MFCD03094776
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₇NO₆
  • Molecular Weight 247.25
  • Synonym(s) D-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-methyl ester
  • SMILES CC(C)(OC(N[C@@H](C(OC)=O)CC(O)=O)=O)C

Description

Boc-D-Asp-OMe features a protected D-aspartic acid side chain with a methyl ester group, enabling stable incorporation into peptide sequences. The Boc group ensures efficient deprotection under mild acidic conditions, while the methyl ester enhances solubility and compatibility in synthetic workflows. This derivative supports robust peptide synthesis with minimal epimerization risk.

Application

Boc-D-Asp-OMe serves as a key chiral building block for the synthesis of D-aspartic acid-containing peptides and peptidomimetics. The Boc group provides reliable protection of the α-amino function, while the methyl ester facilitates selective hydrolysis or derivatization. This derivative exhibits excellent bench stability, simplifies purification, and enables efficient coupling in standard solid-phase and solution-phase peptide synthesis workflows.

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

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Computational Chemistry Data

  • TPSA   101.93
  • LogP   0.5274
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   4

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