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Structure of 201473-90-7
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This chiral building block features a fluorenylmethoxycarbonyl-protected amino acid scaffold with defined stereochemistry at both C2 and C3 positions. The Fmoc group enables orthogonal deprotection in peptide synthesis, while the sterically constrained backbone supports efficient coupling and high diastereoselectivity in complex oligomer assembly under standard conditions.
(S)-2,3-Bis((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid serves as a key chiral building block for solid-phase peptide synthesis, enabling efficient incorporation of sterically hindered, enantiomerically pure amino acids. The fluorenylmethoxycarbonyl (Fmoc) groups provide excellent orthogonal protection and are readily removed under mild basic conditions. Its bench-stable, crystalline nature facilitates handling and purification, while the protected side chain supports diverse coupling reactions in standard peptide 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-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: