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Structure of 1279032-69-7
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N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-methyl-D-serine features a fluorenylmethoxycarbonyl (Fmoc) group for orthogonal protection and a methylated hydroxyl, enhancing stability during peptide synthesis. This derivative enables efficient incorporation of D-serine residues with minimized epimerization risks under standard conditions.
N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-methyl-D-serine serves as a key chiral building block in peptide synthesis, enabling the incorporation of D-serine residues with orthogonal protection. The Fmoc group provides stable, base-labile N-protection compatible with standard coupling protocols, while the O-methyl ether offers enhanced stability against hydrolysis and facilitates purification. This derivative enables efficient access to complex peptide scaffolds, particularly in medicinal chemistry campaigns requiring stereocontrolled side-chain modifications.
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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: