(3-Phenoxyphenyl)methyl prop-2-enoate
[CAS# 409325-06-0]

Identification

• Classification: Chemical reagent >> Organic reagent >> Ether
• Name: (3-Phenoxyphenyl)methyl prop-2-enoate
• Molecular Formula: C₁₆H₁₄O₃
• Molecular Weight: 254.28
• CAS Registry Number: 409325-06-0
• SMILES: C=CC(=O)OCC1=CC(=CC=C1)OC2=CC=CC=C2

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H315-H319-H335
• Precautionary Statements: P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Discovory and Applicatios

(3-Phenoxyphenyl)methacrylate-2-enoate is a versatile compound used in polymer synthesis, especially for the development of advanced coatings, adhesives, and resin formulations. The synthesis of (3-phenoxyphenyl)methacrylate-2-enoate stems from the study of acrylates and their applications in polymer chemistry. This compound combines the features of acrylate and phenoxy groups, taking advantage of the reactivity of acrylates and the structural advantages of phenoxy groups. It was introduced as a promising monomer in the late 20th century as interest in developing new materials with superior performance characteristics grew. The acrylate group promotes polymerization, allowing the compound to form long-chain polymers and copolymers. The phenoxyphenyl group enhances the rigidity, thermal stability, and chemical resistance of the resulting polymers.

(3-Phenoxyphenyl)methacrylate-2-enoate is widely used in the formulation of high-performance coatings and paints. It is able to polymerize under UV light or initiators, making it suitable for making durable, weather-resistant coatings. These coatings are used in automotive, marine, and industrial applications where durability and aesthetics are critical. (3-Phenoxyphenyl)methacrylate-2-enoate is used in adhesives that require strong bonds and resistance to environmental factors. Polymers derived from this monomer have excellent adhesion to a variety of substrates, including metals, plastics, and composites, making them valuable in the construction, electronics, and automotive industries.

(3-Phenoxyphenyl)methacrylate-2-enoate is used in the development of optical materials such as lenses and films that require clarity and resistance to UV degradation. The phenoxyphenyl group enhances the polymer's refractive index and optical properties, making it suitable for high-precision optical components and coatings. (3-Phenoxyphenyl)methacrylate-2-enoate is also used in the manufacture of electronic devices and composites. Its thermal stability and chemical resistance help improve the performance and life of components in harsh environments such as electronic circuits and high-strength composites.

The phenoxyphenyl moiety imparts significant chemical resistance to polymers, protecting them from degradation by solvents, acids, and bases. This makes the compound ideal for use in harsh chemical environments where the material must maintain its integrity. It provides enhanced thermal stability, allowing the resulting polymer to perform well at elevated temperatures. This property is critical for applications in the automotive and aerospace industries where materials are exposed to high temperatures.

(3-Phenoxyphenyl)methacrylate-2-enoate can be easily copolymerized with other monomers to create customized polymer systems. This versatility enables chemists to design materials with specific properties for applications ranging from flexible films to rigid coatings. The phenoxyphenyl group can be functionalized to further enhance or modify the properties of the polymer, allowing the development of advanced materials with targeted properties.