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Structure of 127425-74-5
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5-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one features a rigid, electron-deficient indenone core with complementary halogen substituents enabling selective cross-coupling reactions. This bench-stable ketone integrates readily into complex molecular architectures under standard conditions, serving as a key building block in synthetic organic chemistry and medicinal research.
5-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted indenone scaffolds via palladium-catalyzed cross-coupling reactions. Its bromo and fluoro substituents offer orthogonal reactivity for sequential functionalization, while the diketone framework supports enantioselective transformations. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in API development.
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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: