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Structure of 223581-75-7
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Fmoc-L-Phe(3-NH2)-OH features a para-amino-substituted phenylalanine residue with an Fmoc protecting group, enabling efficient solid-phase peptide synthesis. The electron-rich aromatic ring and amine-functionalized side chain facilitate coupling reactions while maintaining stability under standard conditions.
Fmoc-L-Phe(3-NH2)-OH serves as a key building block for the synthesis of peptide conjugates and peptidomimetics, leveraging the ortho-amino functionality for site-specific derivatization. The Fmoc group enables efficient solid-phase peptide synthesis, while the 3-aminophenyl side chain provides a versatile handle for bioconjugation and heterocycle formation. This derivative exhibits excellent bench stability, facilitates straightforward purification, and is compatible with standard coupling protocols in medicinal chemistry 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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: