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Structure of 959573-22-9
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Fmoc-Phe(3-CONH2)-OH features a para-amino substituent on the phenyl ring, enhancing solubility and modulating electronic properties for optimized coupling efficiency. This derivative integrates seamlessly into peptide synthesis workflows, offering improved handling and reduced aggregation during chain elongation.
Fmoc-Phe(3-CONH2)-OH serves as a key building block for the synthesis of peptide libraries and bioactive oligomers, featuring a meta-substituted phenylalanine derivative with a C-terminal amide. The Fmoc group enables efficient N-terminal protection in solid-phase peptide synthesis, while the 3-carboxamide functionality provides enhanced solubility and metabolic stability. This compound exhibits excellent bench stability, tolerates standard coupling conditions, and facilitates orthogonal functionalization in complex sequence assembly.
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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 : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: