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Structure of 162752-17-2
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6-(tert-Butyl)-2,3-dihydro-1H-inden-1-one is a sterically hindered indanone derivative featuring a bulky tert-butyl group at the 6-position. This substitution enhances stability and modulates reactivity in synthetic transformations. The molecule integrates readily into complex scaffolds due to its electron-rich aromatic system and functionalized carbonyl site, enabling efficient coupling reactions under mild conditions.
6-(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 enhances steric bulk and bench stability, while the ketone functionality facilitates nucleophilic additions, reductions, and enolate-mediated transformations. This compound functions reliably in standard coupling and cyclization protocols, supporting scalable synthesis of complex heterocycles and pharmaceutical 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
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: