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Structure of 57224-63-2
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Z-Thr-OMe features a protected threonine residue with a benzoyl (Z) group at the amine and methyl ester (OMe) at the carboxyl terminus. This configuration enables stable incorporation into peptide chains under standard conditions, offering reliable handling and compatibility in solid-phase synthesis workflows.
Z-Thr-OMe serves as a versatile chiral building block in peptide synthesis, enabling efficient incorporation of the threonine side chain with orthogonal protection. The Z (benzyloxycarbonyl) group provides stability during coupling steps and facilitates selective deprotection, while the methyl ester offers convenient downstream conversion to carboxylic acids or amides. Its well-documented reactivity supports high-yielding couplings in standard solid-phase and solution-phase protocols.
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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-H315-H319-H335
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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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Lot numbers can be found on the outside label of a product: