Identification | Back Directory | [Name]
MONO-2-(METHACRYLOYLOXY)ETHYL SUCCINATE | [CAS]
20882-04-6 | [Synonyms]
2-Methacryloyloxyethyl succinate 2-METHACRYLOYLOXYETHYL SUCCINIC ACID Mono[2-(Methacryloxy)ethyl] succinate MONO-2-(METHACRYLOYLOXY)ETHYL SUCCINATE [2-(Methacryloyloxy)-ethyl]-hydrogen succinate Succinic acid 1-[2-(methacryloyloxy)ethyl] ester Succinic acid hydrogen 2-methacryloyloxyethyl ester 3-[[2-(Methacryloyloxy)ethoxy]carbonyl]propionic acid Succinic acid hydrogen 2-(methacryloyloxy)ethyl ester [2-[(2-methyl-1-oxoallyl)oxy]ethyl] hydrogen succinate Succinic acid hydrogen [2-(methacryloyloxy)ethyl] ester Succinic acid hydrogen 1-[2-(methacryloyloxy)ethyl] ester Butanedioicacid,mono[2-[(2-methyl-1-oxo-2-propenyl)oxy]ethyl]ester Butanedioic acid, 1-[2-[(2-methyl-1-oxo-2-propen-1-yl)oxy]ethyl] ester | [EINECS(EC#)]
244-096-4 | [Molecular Formula]
C10H14O6 | [MDL Number]
MFCD00274302 | [MOL File]
20882-04-6.mol | [Molecular Weight]
230.21 |
Hazard Information | Back Directory | [Uses]
mono-2-(Methacryloyloxy)ethyl succinate can be used as:- A monomer to prepare peptide-polymer matrix to fabricate multifunctional adhesive hybrid resin composites for dental restorations. MMES has one carboxylic acid functional group for peptide conjugation and a double bond for copolymerization with the polymer matrix.
- A precursor to synthesize CsPbBr3-based elastomers for flexible optoelectronic devices. The incorporation of MMES helps to improve elasticity, shape recovery, and flexibility.
- A monomer to synthesize poly(MMES-co-GDMA) monosized microbeads to prepare a multifunctional gold nanocatalyst for the removal of organic pollutant 4-Nitrophenol. MMES contributes to the polymer matrix formation, attachment of gold nanoparticles, and enables the catalyst to exhibit magnetic properties.
| [Synthesis]
mono-2-(Methacryloyloxy)ethyl succinate is prepared by the reaction of 2-Hydroxyethyl methacrylate and succinic acid anhydride. The specific synthesis steps are as follows: 10 gm of 2-hydroxyethylmethacrylate, 7.7 gm of succinic anhydride and 50 mg of hydroquinone monomethyl ether were added into a 50m1 flask with a stir bar. The flask was purged with argon, sealed and heated to 90 C with stifling for 18 hours. The flask was cooled to RT to afford mono-2-(Methacryloyloxy)ethyl succinate in quantitative yield.
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