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Structure of 130473-38-0
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This 2,2-dimethyl-6-(2-oxopropyl)-4H-1,3-dioxin-4-one features a sterically hindered dioxinone core with a ketone-functionalized side chain, enabling selective conjugation in synthetic workflows. The electron-deficient ring system facilitates nucleophilic attack, while the dimethyl substitution enhances stability under standard conditions.
2,2-Dimethyl-6-(2-oxopropyl)-4H-1,3-dioxin-4-one serves as a versatile synthon in heterocyclic synthesis, leveraging its α,β-unsaturated γ-lactone framework for Diels-Alder reactions and Michael additions. The gem-dimethyl substitution enhances bench stability and facilitates purification, while the oxopropyl side chain enables downstream functionalization. This scaffold functions reliably in building complex cyclic architectures under standard laboratory conditions.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: