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Structure of 156017-42-4
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N-Fmoc-3-iodo-L-alanine methyl ester features a bench-stable Fmoc protecting group and a reactive iodine substituent at the C3 position, enabling direct late-stage functionalization in peptide synthesis. This electrophilic handle facilitates efficient palladium-catalyzed coupling reactions, streamlining access to non-natural amino acid derivatives for chemical biology and drug discovery applications.
N-Fmoc-3-iodo-L-alanine methyl ester serves as a versatile building block for the synthesis of iodinated amino acid derivatives and peptide conjugates. The Fmoc group enables orthogonal protection in solid-phase peptide synthesis, while the iodine substituent at C3 facilitates late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its methyl ester functionality supports straightforward derivatization and purification, offering excellent bench stability and compatibility with standard synthetic workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: