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Structure of 4160-82-1
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This dihydropyranone derivative features a sterically hindered diketone core with two methyl groups at the 4-position, enhancing stability and modulating reactivity. The fused ring system provides a rigid scaffold ideal for asymmetric synthesis and natural product derivatization under standard conditions.
4,4-Dimethyldihydro-2H-pyran-2,6(3H)-dione serves as a versatile β-keto ester surrogate in synthetic organic chemistry, enabling efficient construction of cyclohexanone and substituted pyran scaffolds. Its enhanced stability and defined stereochemical control facilitate reliable Michael additions, aldol condensations, and heterocycle formation under standard reaction conditions. The molecule functions as a key building block for complex carbocyclic and heterocyclic frameworks relevant to medicinal chemistry and natural product synthesis.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: