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Structure of 6708-37-8
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This bicyclic dienone features a fused 5,6-ring system with enhanced rigidity and defined stereochemistry. The ethano bridge imparts conformational stability, while the quinone functionality enables participation in Diels-Alder reactions and electron transfer processes. Designed for use in synthetic intermediates requiring controlled reactivity and predictable ring strain release.
3a,4,7,7a-Tetrahydro-4,7-ethanoisobenzofuran-1,3-dione serves as a robust bicyclic diester scaffold for synthetic transformations. Its fused ring system provides rigidity and controlled stereochemistry, enabling selective functionalization at C4 and C7 positions. The molecule exhibits excellent bench stability and compatibility with standard coupling reactions, making it a reliable building block for heterocyclic synthesis and complex molecule assembly in medicinal chemistry 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: