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Structure of 55721-65-8
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Boc-D-isoleucine serves as a protected amino acid building block for peptide synthesis, featuring a sterically hindered tert-butoxycarbonyl group that ensures stability during coupling reactions. This derivative enables selective N-terminal protection and facilitates efficient chain elongation under standard conditions.
Boc-D-isoleucine serves as a key chiral building block in peptide synthesis, enabling efficient N-terminal protection with high stability under acidic conditions. Its tert-butoxycarbonyl group facilitates orthogonal deprotection in standard SPPS workflows, while the D-isoleucine side chain provides structural rigidity and resistance to enzymatic degradation. The compound exhibits excellent bench stability, minimal racemization during coupling, and compatibility with diverse activation methods.
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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: