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Structure of 18362-64-6
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This diketone features a sterically shielded central core, enabling stable incorporation into complex synthetic sequences. The methyl groups at C2 and C6 reduce enolization tendencies while maintaining reactivity at the 3,5-dione moiety. Ideal for constructing cyclic architectures under mild conditions.
2,6-Dimethylheptane-3,5-dione serves as a versatile β-diketone scaffold for constructing substituted heterocycles and enantioselective catalysis. Its well-defined diketone functionality enables reliable enolization and metal chelation, facilitating use in transition-metal-catalyzed C–C bond formations. Bench-stable and amenable to standard purification methods, it functions effectively in multistep syntheses requiring functional group tolerance and predictable reactivity.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1224
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: