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Structure of 172169-88-9
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-bromobutanoic acid features a chiral backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling efficient solid-phase peptide synthesis. The pendant bromo substituent provides a handle for downstream functionalization via transition-metal-catalyzed coupling. This derivative combines stability under standard conditions with orthogonal reactivity, facilitating the incorporation of non-canonical amino acids into biologically active peptides.
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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: