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Structure of 1273611-01-0
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5-Bromo-7-chloro-2,3-dihydro-1H-inden-1-one features a rigid, electron-deficient indenone core with strategically positioned halogen substituents. This combination enables direct functionalization in cross-coupling reactions and facilitates incorporation into complex molecular architectures. The molecule exhibits enhanced stability under standard conditions and serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical candidates.
5-Bromo-7-chloro-2,3-dihydro-1H-inden-1-one serves as a versatile building block in medicinal chemistry and synthetic organic research. Its fused bicyclic structure features orthogonal halogen handles—bromine at C5 and chlorine at C7—that enable selective cross-coupling reactions. The ketone functionality facilitates nucleophilic additions and acts as an anchor for further functionalization. Bench-stable and amenable to purification via standard chromatography, it functions effectively in the construction of complex heterocyclic scaffolds and bioactive molecules under mild reaction conditions.
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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: