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Structure of 136497-85-3
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FMOC-SER-OALL features a fluorenylmethoxycarbonyl-protected serine residue with a long-chain alkyne handle, enabling site-specific bioconjugation via copper-catalyzed azide-alkyne cycloaddition. This orthogonal functionality integrates seamlessly into peptide synthesis workflows, offering high chemoselectivity and compatibility with standard coupling conditions.
FMOC-SER-OALL serves as a key building block in peptide synthesis, enabling the site-specific incorporation of serine residues with orthogonal protection. The fluorenylmethyloxycarbonyl (Fmoc) group provides efficient, base-labile deprotection under mild conditions, while the OAll (allyl) ester offers high stability and compatibility with diverse coupling protocols. This combination facilitates robust handling, clean purification, and seamless integration into complex peptide sequences.
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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
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Lot numbers can be found on the outside label of a product: