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Structure of 134486-00-3
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This fluoren-9-ylmethoxycarbonyl-protected chiral amino acid derivative features a para-hydroxy-iodophenyl side chain, enabling direct incorporation into peptide syntheses via solid-phase methods. The Cbz-like protecting group ensures stability under standard coupling conditions and facilitates selective deprotection during purification workflows.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxy-3-iodophenyl)propanoic acid serves as a valuable chiral building block for peptide synthesis, enabling efficient incorporation of iodinated phenolic side chains. The Fmoc group provides excellent stability and orthogonal deprotection, while the 4-hydroxy-3-iodophenyl moiety offers a versatile handle for late-stage functionalization via cross-coupling. Bench-stable and readily purified by chromatography, it facilitates robust access to complex bioactive scaffolds in medicinal chemistry and API development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: