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Structure of 205526-36-9
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This fluorenylmethoxycarbonyl-protected amino acid bears a chiral center at the alpha position, integrating a para-cyanophenyl group for enhanced electronic effects. The (S)-configuration ensures stereochemical fidelity in peptide synthesis, while the fluoren-9-ylmethoxycarbonyl moiety enables efficient orthogonal protection and clean deprotection under mild conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-cyanophenyl)propanoic acid serves as a valuable chiral building block for peptide synthesis and medicinal chemistry applications. The Fmoc-protected amino acid exhibits excellent bench stability, facilitates straightforward purification via flash chromatography, and enables efficient coupling reactions with broad functional group tolerance. Its 3-cyanophenyl side chain provides a versatile handle for downstream modifications, making it well-suited for constructing bioactive scaffolds in drug discovery programs.
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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: