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Structure of 1251904-51-4
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This fluorenylmethoxycarbonyl-protected amino acid features a terminal alkene for downstream functionalization, offering enhanced stability and compatibility in peptide synthesis. The (S)-configuration ensures stereochemical fidelity in chiral building blocks.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)oct-7-enoic acid serves as a valuable chiral building block for peptide synthesis, enabling efficient incorporation of unsaturated amino acid motifs. The Fmoc group provides excellent stability and orthogonal deprotection under mild basic conditions, while the terminal alkene supports downstream functionalization via metathesis or hydrogenation. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for 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: