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Structure of 5411-61-0
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4-Bromo-7-methoxy-2,3-dihydro-1H-inden-1-one features a brominated indenone core with a methoxy group at the 7-position, offering a sterically accessible carbonyl for nucleophilic addition. This bench-stable scaffold integrates readily into complex molecular architectures, enabling efficient access to functionalized heterocycles in synthetic and medicinal chemistry workflows.
4-Bromo-7-methoxy-2,3-dihydro-1H-inden-1-one serves as a versatile building block in the synthesis of biologically active indenone derivatives. Its bromine and methoxy substituents enable selective cross-coupling reactions and functional group transformations, while the ketone moiety facilitates nucleophilic additions and cyclizations. The compound exhibits good bench stability and is compatible with standard synthetic workflows, making it a practical intermediate for medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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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-H401-H411
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Precautionary Statements : P264-P270-P273-P391-P501
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Lot numbers can be found on the outside label of a product: