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Structure of 122889-11-6
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This fluorenylmethoxycarbonyl-protected D-serine derivative features a benzyl ester group for orthogonal deprotection. The Fmoc moiety enables efficient solid-phase peptide synthesis, while the phenylmethyl group provides selective stability under standard conditions. This combination facilitates precise incorporation of D-serine residues in complex peptide sequences.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-O-(phenylmethyl)-D-serine serves as a versatile, bench-stable amino acid derivative for peptide synthesis, enabling efficient Nα- and O-protected D-serine incorporation. The Fmoc group facilitates orthogonal deprotection under mild basic conditions, while the benzyl ester provides excellent stability and compatibility with standard coupling protocols. This reagent supports high-yielding amide bond formation in solid-phase and solution-phase workflows, offering reliable functionality for the construction of complex peptide sequences and peptidomimetics.
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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: