Description
2-[(Oxolan-2-yl)methoxy]ethyl prop-2-enoate (CAS No. 79252-75-8) is a high-purity specialty chemical with the molecular formula C10H16O4, designed for advanced research and industrial applications. This compound, also known by its IUPAC name 2-(oxolan-2-ylmethoxy)ethyl prop-2-enoate, features a unique molecular structure combining an oxolane (tetrahydrofuran) ring with an acrylate ester functionality, making it a versatile intermediate for polymerization and organic synthesis. Its reactive acrylate group enables cross-linking and copolymerization, while the ether linkage enhances solubility and compatibility with various organic matrices. Supplied as a clear, colorless to pale yellow liquid with ≥95% purity (GC), it is rigorously tested for consistency and stability under recommended storage conditions (2-8°C under inert atmosphere). Ideal for photoresists, adhesives, and specialty coatings research. Hazardous: Handle with appropriate PPE.
Properties
- CAS Number: 79252-75-8
- Complexity: 191
- IUPAC Name: 2-(tetrahydrofuran-2-ylmethoxy)ethyl prop-2-enoate
- InChI: InChI=1S/C10H16O4/c1-2-10(11)14-7-6-12-8-9-4-3-5-13-9/h2,9H,1,3-8H2
- InChI Key: JLZQMKLXOVLQFA-UHFFFAOYSA-N
- Exact Mass: 200.10485899
- Molecular Formula: C10H16O4
- Molecular Weight: 200.23
- SMILES: C=CC(=O)OCCOCC1CCCO1
- Topological: 44.8
- Monoisotopic Mass: 200.10485899
- Synonyms: 79252-75-8, 2-[(Oxolan-2-yl)methoxy]ethyl prop-2-enoate, SCHEMBL233284, DTXSID60608869, JLZQMKLXOVLQFA-UHFFFAOYSA-N
Application
This acrylate-functionalized oxolane derivative is primarily employed as a reactive diluent in UV-curable resins and adhesives, where it improves flexibility and adhesion to polar substrates. Researchers utilize it as a building block for synthesizing functional polymers with tailored hydrophilicity and Tg properties. In material science, it serves as a cross-linker for creating hydrogels with enhanced mechanical stability. Not evaluated for pharmaceutical or food applications.
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