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Structure of 205526-23-4
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Fmoc-D-Phe(3-Cl)-OH features a fluorophore-masked D-phenylalanine scaffold with a chlorine atom at the meta position of the aromatic ring. This configuration enhances electron-withdrawing character and improves stability during solid-phase peptide synthesis. The protected side chain resists racemization, enabling reliable incorporation into challenging sequences.
Fmoc-D-Phe(3-Cl)-OH serves as a key building block for the synthesis of peptide-based therapeutics and cyclic peptide scaffolds. The 3-chloro substitution on the phenyl ring enhances metabolic stability and modulates lipophilicity, while the Fmoc group enables efficient solid-phase peptide synthesis. This derivative exhibits excellent bench stability, straightforward purification, and compatibility with standard coupling protocols, facilitating reliable incorporation into complex 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 : H302-H315-H319-H335
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Precautionary Statements : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P340-P362-P403-P405-P501
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Lot numbers can be found on the outside label of a product: