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CS-W001157 4
Total: USD 88.00

Boc-Asp-OMe

  • CAS No. 98045-03-5

  • Cat. No. CS-W019527
  • Purity≥97%
  • MDL No.MFCD03094777

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

Boc-Asp-OMe|CS-W019527

Structure of 98045-03-5

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General Information

  • CAS No. 98045-03-5
  • Cat. No. CS-W019527
  • Purity ≥97%
  • MDL No. MFCD03094777
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₇NO₆
  • Molecular Weight 247.25
  • Synonym(s) None
  • SMILES O=C(O)C[C@H](NC(OC(C)(C)C)=O)C(OC)=O

Description

Boc-Asp-OMe features a tert-butoxycarbonyl-protected aspartic acid methyl ester core, enabling stable incorporation into peptide synthesis sequences. The Boc group ensures efficient N-terminal protection under mild acidic conditions, while the methyl ester facilitates selective deprotection and downstream coupling. This derivative delivers high compatibility with standard solid-phase protocols and supports reliable chain elongation in complex peptide assembly.

Application

Boc-Asp-OMe serves as a key building block in peptide synthesis, enabling efficient incorporation of aspartic acid derivatives with orthogonal protection. The Boc group provides stable Nα protection under acidic conditions, while the methyl ester facilitates selective hydrolysis and subsequent coupling reactions. This di-functionalized scaffold exhibits excellent bench stability, simplifies purification, and supports diverse transformations in solid-phase and solution-phase syntheses.

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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