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Structure of 2922-40-9
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H-DL-Phe(4-NO2)-OH features a para-nitro-substituted phenylalanine scaffold with enhanced electron-withdrawing character, enabling precise tuning of reactivity in peptide synthesis. This bench-stable derivative integrates readily into complex sequences under standard conditions, offering improved solubility and compatibility in aqueous and organic media.
H-DL-Phe(4-NO₂)-OH serves as a versatile building block for peptide synthesis, enabling the incorporation of a para-nitrophenylalanine residue with defined stereochemistry. The nitro group provides a robust handle for downstream transformations, including reduction to an amino group or participation in metal-catalyzed coupling reactions. Its stability under standard peptide coupling conditions and compatibility with common protecting group strategies make it a practical choice for synthesizing functionalized peptides and heterocyclic scaffolds.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: