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Structure of 869494-16-6
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tert-Butyl 3,6-diazabicyclo[3.1.1]heptane-6-carboxylate features a rigid bicyclic scaffold with two nitrogen atoms positioned for strategic coordination and functionalization. This bench-stable, moisture-tolerant reagent integrates readily into medicinal chemistry campaigns, enabling efficient access to constrained heterocyclic architectures through straightforward deprotection or coupling reactions.
tert-Butyl 3,6-diazabicyclo[3.1.1]heptane-6-carboxylate serves as a conformationally constrained diamine building block, enabling efficient access to nitrogen-rich heterocycles in medicinal chemistry. The protected amine functionality offers excellent bench stability and compatibility with standard coupling reactions, while the bicyclic core provides defined spatial orientation for target-directed synthesis. Its robust functional group tolerance facilitates downstream transformations essential in API development workflows.
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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: