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Structure of 609768-49-2
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Boc-D-Cyclopropylglycine features a sterically constrained cyclopropyl ring fused to a D-configured glycine backbone, delivering enhanced conformational rigidity. This structural motif enables precise control in peptide synthesis, particularly for incorporating non-canonical amino acids into bioactive sequences. The Boc protecting group ensures stability during coupling steps and facilitates straightforward deprotection under mild acidic conditions.
Boc-D-Cyclopropylglycine serves as a valuable chiral building block for the synthesis of bioactive peptides and peptidomimetics. The cyclopropyl group imparts conformational rigidity, enhancing target binding affinity in medicinal chemistry applications. The Boc protecting group ensures stability during peptide coupling sequences and facilitates straightforward deprotection under mild acidic conditions. This derivative exhibits excellent functional group tolerance and is compatible with standard solid-phase and solution-phase synthesis protocols.
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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: