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Structure of 102971-73-3
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This fluorenylmethoxycarbonyl-protected cysteine derivative features a sterically hindered tert-butoxy-ketone side chain, enabling selective conjugation in peptide synthesis. The fluoren-9-ylmethoxycarbonyl group ensures efficient N-terminal protection, while the reactive thiol moiety facilitates site-specific bioconjugation under mild conditions.
N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(4-(tert-butoxy)-4-oxobutyl)-L-cysteine serves as a protected cysteine building block for peptide synthesis, enabling selective side-chain functionalization. The Fmoc group provides orthogonal protection for the amine, while the tert-butyl ester and ketone functionalities allow for subsequent derivatization via reductive amination or nucleophilic addition. Bench-stable and compatible with standard coupling protocols, it facilitates efficient incorporation into complex peptide scaffolds and heterocyclic systems.
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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: