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*For research and further manufacturing use only, not for direct human use.
Structure of 352525-25-8
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(pyridin-3-yl)phenyl)propanoic acid features a chiral α-amino acid core with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct use in solid-phase peptide synthesis. The para-pyridinyl-substituted aryl side chain imparts enhanced solubility and stability under standard coupling conditions. This derivative integrates seamlessly into peptide chains with minimal epimerization risk.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(pyridin-3-yl)phenyl)propanoic acid serves as a valuable chiral building block in peptide synthesis and medicinal chemistry. The Fmoc group enables efficient solid-phase peptide coupling, while the phenylpyridine side chain provides a rigid, polar scaffold for drug discovery applications. Its bench-stable nature and compatibility with standard deprotection protocols facilitate reliable incorporation into complex molecular architectures.
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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: