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Structure of 866862-25-1
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5-Bromo-6-fluoro-2,3-dihydro-1H-inden-1-one features a sterically constrained indenone core with complementary halogen substituents. The bromine and fluorine atoms enable selective cross-coupling reactions, while the saturated ring system ensures stability under standard conditions. This scaffold serves as a key intermediate in the synthesis of bioactive molecules and functional materials.
5-Bromo-6-fluoro-2,3-dihydro-1H-inden-1-one serves as a versatile building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its ortho-halogenated indanone core enables palladium-catalyzed cross-coupling reactions with high functional group tolerance. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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: