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Structure of 19943-16-9
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This piperazine-2,5-dione scaffold features a sterically hindered, chiral core with two isopropyl substituents at the 3 and 6 positions, enhancing conformational rigidity and metabolic stability. The fused diketone system enables selective engagement in asymmetric synthesis and molecular scaffold design, particularly in bioactive compound development where controlled stereochemistry and reduced flexibility are critical.
(3S,6S)-3,6-Diisopropylpiperazine-2,5-dione serves as a stereochemically defined, bench-stable building block for the synthesis of complex nitrogen-containing scaffolds. Its rigid, chiral piperazine core enables controlled functionalization in medicinal chemistry campaigns, particularly in the construction of heterocyclic motifs with enhanced metabolic stability. The diisopropyl substituents provide steric protection and improve solubility, facilitating purification and compatibility in multi-step sequences.
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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: