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Structure of 122848-57-1
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6-Boc-3,6-diazabicyclo[3.2.0]heptane delivers a sterically constrained, bench-stable scaffold for asymmetric synthesis and catalysis. The Boc-protected diamine moiety enables sequential functionalization while maintaining solubility in common organic solvents. This bicyclic core integrates seamlessly into ligand design and reagent development, offering precise spatial control over coordination environments.
6-Boc-3,6-diazabicyclo[3.2.0]heptane serves as a robust, bench-stable scaffold for the construction of nitrogen-rich heterocycles in medicinal chemistry. Its protected diamine functionality enables selective functionalization and orthogonal deprotection, facilitating access to diverse bicyclic amine derivatives. The Boc group ensures excellent stability during synthesis and purification, while the rigid bicyclic framework provides defined stereochemistry and conformational restraint—key attributes for optimizing ligand-receptor interactions in target-directed synthesis.
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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: