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Structure of 4427-92-3
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4-Phenyl-1,3-dioxolan-2-one serves as a reactive synthon in carbonyl chemistry, featuring a strained five-membered cyclic anhydride ring that readily undergoes nucleophilic ring opening. The phenyl group enhances electronic stabilization while maintaining high reactivity under mild conditions. This compound integrates efficiently into complex molecular architectures and is particularly valuable in the synthesis of chiral building blocks and functionalized heterocycles.
4-Phenyl-1,3-dioxolan-2-one serves as a stable, bench-accessible synthon for the construction of γ-lactones and functionalized heterocycles. Its cycloaddition reactivity with nucleophiles enables efficient access to chiral building blocks, while its compatibility with common protecting groups facilitates multistep synthesis. The molecule functions as a versatile intermediate in the development of bioactive scaffolds and synthetic intermediates requiring controlled stereochemistry and functional group tolerance.
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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: