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Structure of 1363210-41-6
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This bicyclic scaffold features a protected azabicyclo[2.2.1]heptane core with a tert-butyloxycarbonyl group at the 2-position and a carboxylic acid at the 5-position, enabling direct incorporation into peptide synthesis and medicinal chemistry campaigns.
2-(tert-Butoxycarbonyl)-2-azabicyclo[2.2.1]heptane-5-carboxylic acid serves as a robust, bench-stable building block for the synthesis of constrained azabicyclic scaffolds. The tert-butyl ester group enables straightforward deprotection under mild acidic conditions, while the carboxylic acid functionality supports efficient coupling reactions. Its rigid bicyclic core provides defined stereochemistry and conformational restraint, facilitating use in medicinal chemistry campaigns targeting G-protein-coupled receptors and other structurally sensitive biological targets.
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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: