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Structure of 27611-39-8
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5-Bromo-1H-indene-1,3(2H)-dione features a brominated indenone core with enhanced reactivity at the carbonyl positions. This electron-deficient scaffold integrates readily into cycloaddition and cross-coupling transformations. The bromine substituent enables further functionalization via palladium-catalyzed reactions, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical process development.
5-Bromo-1H-indene-1,3(2H)-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized heterocyclic scaffolds. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the diketone moiety supports enolization and condensation processes. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it valuable for medicinal chemistry campaigns and process-scale synthesis.
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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: