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Structure of 210282-32-9
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Fmoc-Phe(2-I)-OH features a para-iodinated phenylalanine derivative with a fluorenylmethoxy carbonyl (Fmoc) protecting group. This electron-deficient aromatic moiety enhances coupling efficiency in solid-phase peptide synthesis, while the iodine substituent enables downstream functionalization via cross-coupling reactions. The compound exhibits excellent stability under standard handling conditions.
Fmoc-Phe(2-I)-OH serves as a valuable building block in peptide synthesis, enabling the incorporation of iodinated phenylalanine residues. The ortho-iodo substitution provides a versatile handle for subsequent transition-metal-catalyzed functionalization, including cross-coupling reactions. Its stability under standard Fmoc-based solid-phase synthesis conditions and ease of purification make it well-suited for the construction of complex peptide architectures and bioactive scaffolds.
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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: