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Structure of 270262-98-1
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This fluorenylmethoxycarbonyl-protected amino acid features a chiral (S)-configuration and incorporates a thiophene-containing side chain, enabling direct integration into peptide synthesis. The fluorenylmethoxycarbonyl group ensures efficient coupling and selective deprotection under mild conditions.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(thiophen-2-yl)butanoic acid serves as a valuable chiral building block in peptide synthesis, enabling efficient incorporation of β-amino acid motifs with defined stereochemistry. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability under basic conditions and facilitates straightforward removal during solid-phase synthesis. Its thiophene-containing side chain offers a robust platform for diversification via standard coupling reactions, with high functional group tolerance and compatibility across common synthetic 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-P363-P501
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Lot numbers can be found on the outside label of a product: