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Structure of 134003-84-2
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This chiral bicyclic amine scaffold features a rigid, electron-deficient 2,5-diazabicyclo[2.2.1]heptane core with a tert-butyl ester group at the 2-position, enabling selective functionalization in asymmetric synthesis. The (1R,4R) stereochemistry imparts defined spatial orientation for controlled reactivity in catalytic and medicinal chemistry applications.
(1R,4R)-tert-Butyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate serves as a rigid, chiral diamine scaffold enabling stereocontrolled synthesis of bioactive molecules. Its bicyclic structure confers conformational stability and facilitates selective functionalization at nitrogen sites. The tert-butyl ester group provides bench stability and simplifies purification, while the protected amine handles are compatible with standard coupling and reduction protocols. Functions effectively in asymmetric catalysis and as a building block for heterocyclic scaffolds in medicinal chemistry.
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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: