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Structure of 77119-84-7
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Methyl (tert-butoxycarbonyl)-D-phenylalaninate serves as a protected D-phenylalanine derivative, featuring a stable tert-butoxycarbonyl group that enables selective deprotection during peptide synthesis. This bench-stable, moisture-tolerant reagent integrates seamlessly into solid-phase and solution-phase protocols, delivering high functional group fidelity for the construction of bioactive peptides and peptidomimetics.
Methyl (tert-butoxycarbonyl)-D-phenylalaninate serves as a key chiral building block in peptide synthesis, offering D-phenylalanine functionality with orthogonal protection. The tert-butoxycarbonyl (Boc) group provides excellent stability under basic conditions and facilitates mild deprotection with trifluoroacetic acid. Its methyl ester moiety enables direct coupling without additional activation steps, while the phenyl side chain supports efficient incorporation into peptidomimetics and bioactive scaffolds. This compound exhibits high bench stability and ease of purification, making it well-suited for both academic and industrial synthetic 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: