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Structure of 210282-33-0
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Fmoc-Phe(3-COOtBu)-OH features a para-substituted phenylalanine derivative with a tert-butyl ester at the meta position, enabling selective deprotection during peptide synthesis. This configuration enhances solubility and stability under standard coupling conditions, facilitating efficient incorporation into challenging sequences.
Fmoc-Phe(3-COOtBu)-OH serves as a key building block in peptide synthesis, enabling the incorporation of ortho-substituted phenylalanine residues with enhanced solubility and reduced aggregation. The tert-butyl ester group provides stable protection for the carboxylic acid under standard coupling conditions, while the Fmoc group ensures efficient orthogonal deprotection. This derivative facilitates reliable N-terminal capping and supports the synthesis of complex peptide architectures, including those involving sterically hindered or aromatic side chains.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: