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Structure of 500556-91-2
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This rel-((1R,2S,4S)-7-(tert-butoxycarbonyl)-7-azabicyclo[2.2.1]heptane-2-carboxylic acid) features a rigid, bicyclic scaffold with stereochemical control critical for conformationally constrained peptide mimetics. The tert-butoxycarbonyl group provides a stable, orthogonal protecting group for amine incorporation during synthetic sequences.
rel-((1R,2S,4S)-7-(tert-Butoxycarbonyl)-7-azabicyclo[2.2.1]heptane-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of bioactive nitrogen-containing heterocycles. The tert-butyl ester group enables convenient protection and orthogonal deprotection, while the bicyclic scaffold provides conformational rigidity ideal for medicinal chemistry campaigns. It functions effectively in amide coupling and hydrogenation reactions, offering reliable access to complex scaffolds with controlled stereochemistry.
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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: