Description
Dimethyl 2,5-Dioxahexanedioate (CAS: 88754-66-9) is a high-purity organic compound with the molecular formula C6H10O6. This versatile ester derivative is widely utilized in pharmaceutical synthesis, polymer chemistry, and specialty chemical applications due to its unique bifunctional carbonate structure. The compound appears as a clear to pale yellow liquid (or low-melting solid) with excellent solubility in common organic solvents. Our product is rigorously tested to ensure ≥98% purity (GC) and is supplied with comprehensive analytical documentation including HPLC, GC-MS, and NMR spectra. Available in research quantities (100mg-10g) or bulk scale (100g-1kg+), this chemical is packaged under inert atmosphere to ensure stability and longevity. Shelf life is typically 24 months when stored at 2-8°C in the original sealed container.
Properties
- CAS Number: 88754-66-9
- Complexity: 136
- IUPAC Name: 2-methoxycarbonyloxyethyl methyl carbonate
- InChI: InChI=1S/C6H10O6/c1-9-5(7)11-3-4-12-6(8)10-2/h3-4H2,1-2H3
- InChI Key: DOMLQXFMDFZAAL-UHFFFAOYSA-N
- Exact Mass: 178.04773803
- Molecular Formula: C6H10O6
- Molecular Weight: 178.14
- SMILES: COC(=O)OCCOC(=O)OC
- Topological: 71.1
- Monoisotopic Mass: 178.04773803
- Synonyms: 88754-66-9, 2,5-Dioxahexanedioic Acid Dimethyl Ester, Dimethyl 2,5-Dioxahexanedioate, 2-methoxycarbonyloxyethyl methyl carbonate, ethane-1,2-diyl dimethyl dicarbonate, 2,5-DIOXAHEXANEDIOICACIDDIMETHYLESTER, NSC97193, MFCD00085447, SCHEMBL47896, DTXSID20294585, NDA75466, NSC-97193, AKOS015840251, Ethane-1,2-diyl dimethyl bis(carbonate), BS-44080, CS-0330558, D2455, ETHYLENE GLYCOL BIS-(METHYL CARBONATE), D90066
Dimethyl 2,5-Dioxahexanedioate serves as a valuable building block in organic synthesis, particularly for creating carbonate-linked polymer backbones. Its bifunctional nature makes it ideal for step-growth polymerization reactions to produce polycarbonates with tailored properties. The compound has shown utility as a protecting group reagent in nucleoside chemistry and as a precursor for electrolyte additives in advanced battery systems. Researchers also employ this diester in the development of prodrug formulations due to its hydrolytic cleavage characteristics under physiological conditions.
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