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Structure of 219967-68-7
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoic acid features a chiral backbone with orthogonal protecting groups: the Fmoc moiety enables efficient N-terminal protection in peptide synthesis, while the Boc group stabilizes the side-chain amine. This combination supports selective coupling reactions under mild conditions, delivering high fidelity in sequence assembly.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoic acid serves as a key chiral building block for the synthesis of peptide-based intermediates and bioactive molecules. The Fmoc group enables efficient N-terminal protection with orthogonal deprotection, while the Boc-labeled side chain amine supports selective functionalization. Its bench-stable nature and compatibility with standard coupling protocols facilitate streamlined solid-phase and solution-phase peptide synthesis workflows.
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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: