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Structure of 1260018-10-7
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5-Bromo-6-chloro-2,3-dihydro-1H-inden-1-one features a sterically constrained indenone core with complementary halogen substituents at the 5- and 6-positions. This electron-deficient scaffold enables direct functionalization in transition-metal-catalyzed cross-coupling reactions and serves as a key intermediate in the synthesis of biologically active heterocycles.
5-Bromo-6-chloro-2,3-dihydro-1H-inden-1-one serves as a versatile building block for the synthesis of substituted indene derivatives and heterocyclic scaffolds. Its dual halogen substituents enable efficient cross-coupling reactions, while the ketone functionality supports nucleophilic additions and condensation processes. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows requiring ortho-functionalized indenone intermediates.
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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: