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Structure of 1257849-07-2
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Fmoc-5-Chloro-L-tryptophan integrates a chlorinated indole ring into peptide synthesis, enabling site-specific incorporation of electron-deficient tryptophan derivatives. This bench-stable reagent facilitates the introduction of halogenated functionalities for probing protein structure and function, particularly in studies requiring enhanced photoreactivity or metabolic labeling.
Fmoc-5-Chloro-L-tryptophan serves as a valuable building block for peptide synthesis, enabling the incorporation of a halogenated tryptophan residue with enhanced electronic and steric properties. The Fmoc group provides reliable orthogonal protection for the amine, while the 5-chloro substitution offers a versatile handle for downstream functionalization via cross-coupling or nucleophilic substitution. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient solid-phase and solution-phase synthesis workflows.
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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: