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Structure of 1233495-02-7
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Fmoc-β-D-HoTyr(tBu)-OH is a stereochemically defined amino acid derivative featuring a β-hydroxytyrosine scaffold with a tert-butyl protected phenolic hydroxyl. This bench-stable building block integrates readily into peptide chains, enabling the introduction of a polar, hydrogen-bonding moiety at defined positions within synthetic sequences.
Fmoc-β-D-HoTyr(tBu)-OH serves as a valuable building block for the synthesis of peptide conjugates and peptidomimetics, enabling site-specific incorporation of β-hydroxytyrosine derivatives. The Fmoc group provides orthogonal protection for amine functionality, while the tert-butyl ether ensures stability during standard solid-phase peptide synthesis. Its D-stereoisomer configuration offers enhanced metabolic resistance, and the β-hydroxyl group facilitates downstream functionalization or hydrogen bonding in bioactive scaffolds.
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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: