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Atomfair 4,5-Divinyl-1,3-dioxolan-2-one C7H8O3

Description 4,5-Divinyl-1,3-dioxolan-2-one (CAS: 15896-04-5) is a high-purity cyclic carbonate derivative with the molecular formula C7H8O3. This specialized chemical features a 1,3-dioxolan-2-one core substituted with vinyl groups at the 4 and 5 positions, offering unique reactivity for advanced organic synthesis. With an IUPAC name of 4,5-bis(ethenyl)-1,3-dioxolan-2-one , this compound is characterized by its dual vinyl functionality which enables participation in polymerization reactions and serves as a versatile building block for functional materials. Our product is rigorously analyzed by GC/MS, NMR, and HPLC to ensure >98% purity, meeting the stringent requirements of pharmaceutical research, polymer chemistry, and materials science applications. Supplied in…

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Description

Description

4,5-Divinyl-1,3-dioxolan-2-one (CAS: 15896-04-5) is a high-purity cyclic carbonate derivative with the molecular formula C7H8O3. This specialized chemical features a 1,3-dioxolan-2-one core substituted with vinyl groups at the 4 and 5 positions, offering unique reactivity for advanced organic synthesis. With an IUPAC name of 4,5-bis(ethenyl)-1,3-dioxolan-2-one, this compound is characterized by its dual vinyl functionality which enables participation in polymerization reactions and serves as a versatile building block for functional materials. Our product is rigorously analyzed by GC/MS, NMR, and HPLC to ensure >98% purity, meeting the stringent requirements of pharmaceutical research, polymer chemistry, and materials science applications. Supplied in amber glass vials under inert atmosphere to prevent premature polymerization.

  • CAS No: 15896-04-5
  • Molecular Formula: C7H8O3
  • Molecular Weight: 140.14
  • Exact Mass: 140.047344113
  • Monoisotopic Mass: 140.047344113
  • IUPAC Name: 4,5-bis(ethenyl)-1,3-dioxolan-2-one
  • SMILES: C=CC1C(OC(=O)O1)C=C
  • Synonyms: 4,5-divinyl-1,3-dioxolan-2-one, 15896-04-5, DTXSID60470003, DTXCID60420821, SCHEMBL471971

Application

This vinyl-functionalized cyclic carbonate serves as a key monomer for designing cross-linkable polymer networks, particularly in dental resins and specialty coatings. Researchers utilize its dual reactivity (cyclic carbonate + vinyl groups) for developing advanced electrolyte materials in lithium-ion batteries. The compound also finds use as a precursor for synthesizing functionalized polycarbonates with tailored thermal and mechanical properties.

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