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Structure of 1260011-83-3
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7-Bromo-6-fluoro-2,3-dihydro-1H-inden-1-one features a rigid, electron-deficient indenone core with orthogonal halogen substituents enabling selective functionalization. This bench-stable ketone integrates readily into transition-metal-catalyzed coupling cascades and serves as a key scaffold for bioactive heterocycle synthesis.
7-Bromo-6-fluoro-2,3-dihydro-1H-inden-1-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of bioactive heterocycles through palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its ortho-halogenated indenone scaffold offers excellent functional group tolerance and bench stability, facilitating downstream derivatization in API development 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: