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Structure of 130674-54-3
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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.
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.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: