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Structure of 133565-45-4
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This fluoren-9-ylmethoxycarbonyl-protected hydroxyproline derivative features a stereodefined (S)-configuration and a bench-stable tert-butyl ester, enabling direct incorporation into peptide chains under standard coupling conditions. The orthogonal protecting groups facilitate selective deprotection during synthetic workflows.
tert-Butyl (S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-hydroxybutanoate serves as a protected hydroxy amino acid building block for peptide synthesis, enabling the incorporation of (S)-4-hydroxyproline motifs. The Fmoc group provides orthogonal protection for the amine, while the tert-butyl ester allows selective deprotection under mild acidic conditions. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient solid-phase and solution-phase peptide assembly.
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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: