2653-39-6

Usage

Uses

Used in Plastics and Resin Industry:
[(4-Ethenylphenoxy)methyl]oxirane is used as a monomer for the production of various types of plastics and resins. Its application is based on its ability to polymerize and form stable, durable materials with a wide range of properties suitable for different applications.
Used in Synthetic Rubber Industry:
In the synthetic rubber industry, [(4-Ethenylphenoxy)methyl]oxirane is used as a key component in the synthesis of rubber materials. It contributes to the development of rubber with specific characteristics, such as elasticity and resistance to wear, which are essential for various industrial and consumer products.
Used as a Stabilizer in Material Protection:
[(4-Ethenylphenoxy)methyl]oxirane is utilized as a stabilizer in materials to prevent degradation caused by exposure to oxygen or ultraviolet light. Its role in this application is to enhance the longevity and performance of the materials, thereby reducing the need for frequent replacements and maintenance.

InChI:InChI=1/C11H12O2/c1-2-9-3-5-10(6-4-9)12-7-11-8-13-11/h2-6,11H,1,7-8H2

Upstream product

• 2628-17-3 4-Vinylphenol 
• 106-89-8 epichlorohydrin 
• 107-14-2 chloroacetonitrile 
• 112-55-0 1-dodecylthiol 

Relevant academic research and scientific papers

4-Vinylphenyl Glycidyl Ether: Synthesis, RAFT Polymerization, and Postpolymerization Modifications with Alcohols

4-Vinylphenyl glycidyl ether (4VPGE), an epoxide-containing styrenic monomer, was synthesized and then polymerized in a controlled fashion under reversible addition-fragmentation chain-transfer (RAFT) polymerization conditions using butyl 1-phenylethyl trithiocarbonate as the chain-transfer agent. The high degree of chain-end functionalization of the produced polymers was confirmed by chain extension reactions with styrene that afforded well-defined block copolymers. Phenyl glycidyl ether was utilized as a model compound to identify the optimal reaction conditions for alcoholysis of the glycidyl moiety using BF3 as a Lewis acid catalyst, and postpolymerization modifications were subsequently carried out on the epoxide groups of poly4VPGE with a library of structurally diverse alcohols to yield a number of β-hydroxy ether-functionalized polymers.

METHOD FOR PREPARING GLYCIDYLOXYSTYRENE MONOMERS AND POLYMERS THEREOF

It was found that glycidyloxystyrenes, including glycidyloxystyrene and substituted glycidyloxystyrene, can be synthesized from hydroxycinnamic acid or substituted hydroxycinnamic acids in a one-pot, two-step process. The substrate can be thermally decarboxylated and then without purification, reacted in the presence of a halomethyl-oxirane and a base. The resulting product can be polymerized or coppolymerized to a fully substituted product.