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Structure of 71630-31-4
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tert-Butyl (tert-butoxycarbonyl)-D-serinate features a protected D-serine scaffold with orthogonal reactivity, enabling selective incorporation into peptide sequences. The tert-butoxycarbonyl group ensures stability during synthesis and facilitates straightforward deprotection under mild acidic conditions. This derivative supports efficient access to non-natural amino acid motifs in peptide-based drug discovery and chemical biology applications.
tert-Butyl (tert-butoxycarbonyl)-D-serinate serves as a stable, bench-ready D-amino acid building block for peptide synthesis, enabling selective incorporation of D-serine residues. The Boc group provides excellent protection under standard acidic conditions and facilitates straightforward deprotection during late-stage functionalization. Its compatibility with diverse coupling reagents and tolerance to common functional groups make it a practical choice for constructing bioactive peptides and heterocyclic scaffolds.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: