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Structure of 479064-89-6
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This chiral fluorenonyl-protected amino acid derivative features a sterically hindered, electron-deficient aryl group and a bench-stable carbamate handle. It integrates seamlessly into solid-phase peptide synthesis workflows, enabling efficient incorporation of fluorinated phenylalanine analogs with high enantiocontrol.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-fluorophenyl)propanoic acid serves as a robust chiral building block for the synthesis of biologically active peptides and pharmaceutical intermediates. The Fmoc-protected amino group enables efficient solid-phase peptide synthesis, while the 4-fluorophenyl side chain provides structural rigidity and favorable pharmacokinetic properties. Its bench-stable nature and compatibility with standard coupling conditions facilitate reliable purification and scalable processing in medicinal chemistry 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: