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Structure of 5241-66-7
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Boc-D-Met-OH serves as a protected derivative of D-methionine, enabling direct incorporation into peptide chains without side-chain interference. The tert-butoxycarbonyl group ensures stability during synthesis and facilitates selective deprotection under mild acidic conditions. This residue integrates cleanly into diverse peptide architectures, particularly where stereochemical integrity and metabolic resistance are critical.
Boc-D-Met-OH serves as a protected D-methionine building block for peptide synthesis, enabling selective incorporation of D-Met residues with high stability and ease of deprotection. The tert-butoxycarbonyl (Boc) group offers robust protection under acidic conditions, while the thioether side chain provides functional group tolerance in standard coupling protocols. Its bench-stable solid form facilitates handling and purification, making it well-suited for both manual and automated synthetic workflows in medicinal chemistry and peptide library development.
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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: