Description

2-(2-Vinyloxyethoxy)ethyl methacrylate (CAS No. 76392-22-8) is a high-purity, multifunctional monomer with the molecular formula C₁₀H₁₆O₄. This compound, also known by its IUPAC name 2-(2-ethenoxyethoxy)ethyl 2-methylprop-2-enoate, is a versatile building block for polymer synthesis, offering both vinyl ether and methacrylate functionalities. Its unique structure enables dual reactivity, making it ideal for UV-curable coatings, adhesives, and advanced material applications. The product is rigorously tested for purity and stability, ensuring consistent performance in research and industrial settings. Suitable for free-radical polymerization, it is commonly used to modify polymer backbones for enhanced flexibility, adhesion, and crosslinking density.

Properties

• CAS Number: 76392-22-8
• Complexity: 198
• IUPAC Name: 2-(2-vinyloxyethoxy)ethyl 2-methylprop-2-enoate
• InChI: InChI=1S/C10H16O4/c1-4-12-5-6-13-7-8-14-10(11)9(2)3/h4H,1-2,5-8H2,3H3
• InChI Key: MGMSZKIPUNOMCS-UHFFFAOYSA-N
• Exact Mass: 200.10485899
• Molecular Formula: C10H16O4
• Molecular Weight: 200.23
• SMILES: CC(=C)C(=O)OCCOCCOC=C
• Topological: 44.8
• Monoisotopic Mass: 200.10485899
• Synonyms: 76392-22-8, DTXSID10431164, 2-(2-VINYLOXYETHOXY)ETHYL METHACRYLATE, DTXCID90381996, 2-Propenoic acid, 2-methyl-, 2-[2-(ethenyloxy)ethoxy]ethyl ester, 2-(2-ethenoxyethoxy)ethyl 2-methylprop-2-enoate, SCHEMBL36623, (2-vinyloxy-ethoxy-ethyl) methacrylate, 2-(2′-vinyloxyethoxy)ethyl methacrylate, 2-(2-(Vinyloxy)ethoxy)ethyl methacrylate, 2-[(2-vinyloxy)ethoxy]ethyl methacrylate

Application

This monomer is widely used in UV-curable formulations for coatings, inks, and adhesives due to its dual-reactive groups. It enhances polymer flexibility and crosslinking in acrylic and vinyl ether systems. Researchers also utilize it in specialty polymers for biomedical and electronic applications.

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