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Structure of 4600-86-6
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This sterically hindered indenone features a tert-butyl group at the 5-position, enhancing solubility and stability. The dihydroindene core provides a rigid, electron-rich scaffold ideal for transition metal-catalyzed coupling reactions and synthetic building blocks in complex molecule assembly.
5-(tert-Butyl)-2,3-dihydro-1H-inden-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indane and indenone frameworks. Its tert-butyl group imparts steric bulk and enhanced bench stability, while the ketone functionality supports standard transformations including nucleophilic additions, reductions, and conjugate additions. The molecule functions effectively in catalytic cross-coupling reactions and facilitates the construction of complex heterocyclic scaffolds relevant to medicinal chemistry and process development.
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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: