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Structure of 5455-94-7
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This cyclic ketone features a sterically shielded dihydrofuran ring system, enhancing stability under standard conditions. The tetramethyl substitution pattern imparts high solubility in organic solvents and reduces nucleophilic reactivity at the carbonyl center. This structure enables selective transformations in synthetic sequences requiring robust, bench-stable ketone intermediates.
2,2,5,5-Tetramethyldihydrofuran-3(2H)-one serves as a stable, bench-ready synthon for the construction of substituted pyrrolidines and other nitrogen-containing heterocycles. Its α,α,β,β-tetramethyl substitution enhances kinetic stability and facilitates clean ring-opening reactions with nucleophiles. The molecule functions as a versatile building block in synthetic routes requiring controlled carbonyl reactivity and orthogonal functional group tolerance.
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GHS Pictogram :
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GHS No : GHS02
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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
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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: