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Boc-Ala-Ala-OH

  • CAS No. 27317-69-7

  • Cat. No. CS-0097837
  • Purity≥97%
  • MDL No.MFCD00038564

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

Boc-Ala-Ala-OH|CS-0097837

Structure of 27317-69-7

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General Information

  • CAS No. 27317-69-7
  • Cat. No. CS-0097837
  • Purity ≥97%
  • MDL No. MFCD00038564
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₂₀N₂O₅
  • Molecular Weight 260.29
  • Synonym(s) NSC 334362
  • SMILES C[C@@H](C(O)=O)NC([C@H](C)NC(OC(C)(C)C)=O)=O

Description

Boc-Ala-Ala-OH is a dipeptide derivative featuring a tert-butoxycarbonyl-protected N-terminus and a free C-terminal carboxylic acid. This bench-stable intermediate facilitates efficient coupling reactions in peptide synthesis, enabling straightforward access to longer sequences through iterative condensation protocols.

Application

Boc-Ala-Ala-OH serves as a reliable dipeptide building block for peptide synthesis, offering bench-stable protection of the N-terminus via the Boc group. It facilitates efficient coupling reactions with minimal epimerization and enables straightforward deprotection under mild acidic conditions. The C-terminal carboxylic acid supports direct activation for amide bond formation, making it well-suited for modular assembly of larger peptides and peptidomimetics.

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   104.73
  • LogP   0.4889
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   4

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