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Structure of 203866-15-3
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N-Boc-4,4-difluoro-L-proline serves as a conformationally constrained building block for peptide synthesis, leveraging the rigidity of the proline scaffold enhanced by geminal difluorination. The Boc group provides stable protection under standard deprotection conditions, while the 4,4-difluoro substitution improves metabolic stability and modulates electronic properties. This derivative facilitates efficient incorporation into peptidomimetics and macrocyclic scaffolds, enabling precise control over backbone geometry in medicinal chemistry campaigns.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: