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CS-W001157 4
Total: USD 88.00

Boc-D-Asp-OBzl

  • CAS No. 92828-64-3

  • Cat. No. CS-B1296
  • Purity≥98%
  • MDL No.MFCD00038264

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

Boc-D-Asp-OBzl|CS-B1296

Structure of 92828-64-3

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General Information

  • CAS No. 92828-64-3
  • Cat. No. CS-B1296
  • Purity ≥98%
  • MDL No. MFCD00038264
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₂₁NO₆
  • Molecular Weight 323.34
  • Synonym(s) (R)-2-tert-Butoxycarbonylaminosuccinic acid 1-benzyl ester
  • SMILES O=C(O)C[C@H](C(OCC1=CC=CC=C1)=O)NC(OC(C)(C)C)=O

Description

Boc-D-Asp-OBzl serves as a protected D-aspartic acid derivative for peptide synthesis, featuring a tert-butoxycarbonyl group at the α-amino position and a benzyl ester at the side-chain carboxylate. This configuration enables selective deprotection and coupling under standard conditions, enhancing stability during storage and handling.

Application

Boc-D-Asp-OBzl serves as a versatile dipeptide building block for the synthesis of peptide-based pharmaceuticals and bioactive oligomers. The Boc group provides orthogonal protection for the α-amino function, while the OBzl ester enables selective deprotection under mild conditions. Its stability under standard coupling protocols and compatibility with diverse synthetic workflows make it ideal for solid-phase and solution-phase peptide synthesis.

Safety Information

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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   2.0978
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   6

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