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Structure of 26465-81-6
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This sterically hindered ketone features a fused bicyclic structure with a methyl-substituted indanone core, offering enhanced stability and defined reactivity in transition metal-catalyzed transformations. Its electron-deficient carbonyl site facilitates efficient nucleophilic addition and cycloaddition processes under mild conditions.
3,3-Dimethyl-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 scaffolds. Its stable ketone functionality tolerates diverse reaction conditions, facilitating nucleophilic additions, reductions, and coupling transformations. The sterically hindered dimethyl substitution enhances bench stability and simplifies purification, making it well-suited for iterative synthesis in medicinal chemistry and process 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-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: