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Structure of 863304-76-1
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4-((tert-Butoxycarbonyl)amino)bicyclo[2.2.2]octane-1-carboxylic acid features a rigid bicyclic core that imparts conformational stability, enabling precise spatial orientation in synthetic applications. The tert-butoxycarbonyl group provides a protected amine handle for subsequent deprotection and coupling, while the carboxylic acid moiety supports efficient derivatization under standard conditions. This combination facilitates integration into complex molecular architectures with defined stereochemistry.
4-((tert-Butoxycarbonyl)amino)bicyclo[2.2.2]octane-1-carboxylic acid serves as a stable, bench-accessible building block for the synthesis of constrained amino acid derivatives and peptidomimetics. The tert-butoxycarbonyl (Boc) group provides excellent protection for primary amines during multi-step syntheses, while the rigid bicyclic core imparts conformational constraint ideal for probing bioactive conformations in medicinal chemistry. Its compatibility with standard coupling protocols and ease of deprotection under mild acidic conditions facilitates efficient incorporation into complex molecular architectures.
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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: