Description
Diethyl 2,5-Dioxahexanedioate (CAS No. 35466-87-6) is a high-purity organic compound with the molecular formula C8H14O6. Also known as 2-ethoxycarbonyloxyethyl ethyl carbonate, this ester derivative is widely utilized in synthetic chemistry and material science applications. Its unique structure, featuring two ester functionalities linked by an ether bridge, makes it a versatile building block for polymerization, crosslinking, and specialty chemical synthesis. This product is rigorously tested for quality, ensuring optimal performance in research and industrial settings. Available in various quantities, it is supplied with comprehensive analytical data (including GC/MS, NMR, and HPLC) to meet the stringent requirements of researchers and scientists.
Properties
- CAS Number: 35466-87-6
- Complexity: 159
- IUPAC Name: 2-ethoxycarbonyloxyethyl ethyl carbonate
- InChI: InChI=1S/C8H14O6/c1-3-11-7(9)13-5-6-14-8(10)12-4-2/h3-6H2,1-2H3
- InChI Key: MYNUAGYBVSQRFN-UHFFFAOYSA-N
- Exact Mass: 206.07903816
- Molecular Formula: C8H14O6
- Molecular Weight: 206.19
- SMILES: CCOC(=O)OCCOC(=O)OCC
- Topological: 71.1
- Monoisotopic Mass: 206.07903816
- Synonyms: 35466-87-6, Diethyl 2,5-Dioxahexanedioate, 2,5-Dioxahexanedioic Acid Diethyl Ester, 2-ethoxycarbonyloxyethyl ethyl carbonate, 2,5-DIOXAHEXANEDIOICACIDDIETHYLESTER, Ethane-1,2-diyl diethyl bis(carbonate), MFCD00460005, SCHEMBL1718009, DTXSID00524630, MYNUAGYBVSQRFN-UHFFFAOYSA-N, Ethane-1,2-diyl diethyl biscarbonate, CS-0361309, D2456, D90067
Application
Diethyl 2,5-Dioxahexanedioate is commonly employed as a monomer or crosslinking agent in polymer chemistry, particularly for synthesizing biodegradable or functionalized polyesters. Its dual ester groups enable controlled reactivity in condensation polymerization, making it valuable for designing novel polymeric materials. Researchers also utilize it as a precursor for specialty carbonates or as a solvent additive in electrolyte formulations. Its stability and solubility in organic solvents further broaden its utility in fine chemical synthesis.
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