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CS-W001157 4
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(Tert-butoxycarbonyl)-L-serine hydrate

  • CAS No. 204191-40-2

  • Cat. No. CS-0449492
  • Purity≥95%
  • MDL No.MFCD00150501

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

(Tert-butoxycarbonyl)-L-serine hydrate|CS-0449492

Structure of 204191-40-2

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General Information

  • CAS No. 204191-40-2
  • Cat. No. CS-0449492
  • Purity ≥95%
  • MDL No. MFCD00150501
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₁₇NO₆
  • Molecular Weight 223.22
  • Synonym(s) Boc-L-Serine Hydrate
  • SMILES CC(OC(N[C@@H](CO)C(O)=O)=O)(C)C.O

Description

(Tert-butoxycarbonyl)-L-serine hydrate features a protected amino group and a hydroxyl-bearing side chain, enabling selective derivatization in peptide synthesis. This bench-stable, moisture-tolerant reagent integrates seamlessly into solid-phase workflows, delivering reliable coupling efficiency under standard conditions.

Application

(Tert-butoxycarbonyl)-L-serine hydrate serves as a stable, bench-ready amino acid derivative enabling efficient peptide synthesis. The Boc group provides orthogonal protection for the amine, while the serine side chain hydroxyl remains available for selective functionalization. Its crystalline form and ease of purification facilitate reliable handling in multistep syntheses, making it a practical building block for peptidomimetics and complex heterocyclic scaffolds.

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   127.36
  • LogP   -0.8681
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   3

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