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CS-W001157 4
Total: USD 88.00

Fmoc-D-allo-Thr-OH

  • CAS No. 130674-54-3

  • Cat. No. CS-0655405
  • Purity≥98%
  • MDL No.MFCD01318738

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

Fmoc-D-allo-Thr-OH|CS-0655405

Structure of 130674-54-3

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General Information

  • CAS No. 130674-54-3
  • Cat. No. CS-0655405
  • Purity ≥98%
  • MDL No. MFCD01318738
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₁₉NO₅
  • Molecular Weight 341.36
  • Synonym(s) None
  • SMILES C[C@@H](O)[C@H](C(O)=O)NC(OCC1C2=CC=CC=C2C3=CC=CC=C31)=O

Description

Fmoc-D-allo-Thr-OH is a stereochemically defined amino acid derivative featuring a fluorenylmethoxy carbonyl (Fmoc) protecting group on the α-amino terminus and a hydroxyl-bearing side chain in the D-allo-threonine configuration. This configuration imparts distinct conformational rigidity and enhanced resistance to racemization during peptide synthesis. The molecule integrates readily into solid-phase workflows, where its bench-stable nature and predictable coupling kinetics streamline sequence assembly. Its polar side chain supports solubility in common organic solvents, facilitating handling under standard conditions.

Application

Fmoc-D-allo-Thr-OH serves as a key building block in peptide synthesis, enabling the incorporation of D-allo-threonine residues with high stereochemical fidelity. The Fmoc group provides orthogonal protection for the α-amino function, facilitating efficient stepwise chain elongation. The hydroxyl-bearing side chain offers controlled reactivity for selective derivatization and is compatible with standard coupling conditions, purification workflows, and bench-stable handling in solid-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-H312-H315-H319-H332-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501

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Computational Chemistry Data

  • TPSA   95.86
  • LogP   2.3591
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   5

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