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Structure of 83400-91-3
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Potassium 2,2-dimethyl-1,3-dioxolane-4-carboxylate serves as a stable, bench-ready synthon for constructing complex carbonyl-containing architectures. The cyclic acetal moiety enhances kinetic stability while the carboxylate group enables facile functionalization under mild conditions. This reagent integrates seamlessly into iterative synthesis workflows requiring reliable C–C bond formation.
Potassium 2,2-dimethyl-1,3-dioxolane-4-carboxylate serves as a stable, bench-ready synthon for the stereoselective introduction of α-alkylated carboxylate units in asymmetric synthesis. Its rigid dioxolane framework enhances diastereoselectivity in nucleophilic additions and functions effectively in transition-metal-catalyzed couplings. The potassium salt ensures excellent solubility and compatibility with standard synthetic protocols, facilitating efficient access to functionalized carbonyl derivatives and complex heterocyclic scaffolds.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: