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CS-W001157 4
Total: USD 88.00

(tert-Butoxycarbonyl)-D-aspartic acid

  • CAS No. 62396-48-9

  • Cat. No. CS-0020433
  • Purity≥98%
  • MDL No.MFCD00798618

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

(tert-Butoxycarbonyl)-D-aspartic acid|CS-0020433

Structure of 62396-48-9

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General Information

  • CAS No. 62396-48-9
  • Cat. No. CS-0020433
  • Purity ≥98%
  • MDL No. MFCD00798618
  • 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[C@H](C(O)=O)NC(OC(C)(C)C)=O

Description

Boc-D-aspartic acid serves as a protected derivative for D-aspartate synthesis, featuring a stable tert-butoxycarbonyl group that simplifies purification and handling. This bench-stable reagent integrates efficiently into peptide coupling workflows, enabling selective incorporation of D-aspartic acid residues under standard conditions.

Application

Boc-D-aspartic acid serves as a key building block in peptide synthesis, enabling efficient protection of the α-amino group while maintaining compatibility with standard deprotection conditions. Its tert-butoxycarbonyl (Boc) group provides excellent stability under basic and neutral conditions, facilitating orthogonal handling in multi-step syntheses. The molecule's carboxylic acid functionality supports diverse coupling reactions, making it well-suited for constructing biologically relevant scaffolds, including cyclic peptides and D-amino acid-containing sequences.

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

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