eoeoea monomer ethyl 2 bromomethyl acrylate cas number formula


Ethyl 2 - Bromomethyl Acrylate: A Versatile MonomerEthyl 2-Bromomethyl Acrylate - A Versatile Monomer
Ethyl 2 - bromomethyl acrylate is a compound with unique chemical properties that has found significant applications in various fields.Ethyl 2-bromomethyl-acrylate is a chemical compound with unique properties. It has been used in many fields. It is denoted by a specific CAS number (the CAS number for ethyl 2 - bromomethyl acrylate is 5464 - 58 - 6), which serves as a universal identifier for this chemical in scientific and industrial contexts.It is identified by a CAS number (the number for ethyl 2-bromomethyl-acrylate is 5464-58-6), which is used as a universal identification for this chemical both in scientific and industrial contexts. Its chemical formula is C6H9BrO2.Its chemical name is C6H9BrO2.

This monomer contains a reactive acrylate group and a bromomethyl moiety.This monomer contains an acrylate group that is reactive and a bromomethyl moiety. The acrylate group is well - known for its ability to participate in polymerization reactions.The acrylate moiety is well-known for its ability to participate polymerization reactions. Double bonds in the acrylate group can undergo addition polymerization, allowing ethyl 2 - bromomethyl acrylate to form polymers.Double bonds within the acrylate groups can undergo addition polymerization. This allows ethyl 2-bromomethyl-acrylate to form polymers. These polymers can have a wide range of properties depending on the reaction conditions and the presence of other monomers in a copolymerization process.These polymers have a variety of properties that depend on the reaction conditions as well as the presence of monomers during a copolymerization.

The bromomethyl group in ethyl 2 - bromomethyl acrylate adds another dimension of reactivity.The bromomethyl group adds a new dimension of reactivity to ethyl 2-bromomethyl acrylate. The bromine atom is a good leaving group.The bromine atom makes a good leaving group. This makes the compound useful in substitution reactions.This makes the compound useful for substitution reactions. For example, it can react with nucleophiles.It can, for example, react with nucleophiles. Amines, for instance, can react with ethyl 2 - bromomethyl acrylate in a nucleophilic substitution reaction.Amines can, for example, react with ethyl 2-bromomethylacrylate in a substitution reaction. The nitrogen atom of the amine attacks the carbon atom adjacent to the bromine, displacing the bromide ion.The nitrogen atom in the amine attacks a carbon atom next to the bromine ion, displace the bromide. This reaction can be used to introduce amine - containing functional groups into the polymer chain when ethyl 2 - bromomethyl acrylate is part of a polymer backbone.This reaction can be used when ethyl 2-bromomethyl-acrylate is a part of the polymer backbone to introduce amine-containing functional groups.

In the field of materials science, polymers derived from ethyl 2 - bromomethyl acrylate can be used to create functional materials.Polymers derived from ethyl 2-bromomethyl-acrylate can be used in materials science to create functional materials. The reactive bromomethyl groups can be further modified to introduce different types of functionality.The bromomethyl groups that react with each other can be further modified in order to introduce different functionality. For example, they can be used to attach fluorescent dyes or other types of probes.They can be used, for example, to attach fluorescent dyes and other types of probes. This can be highly beneficial in applications such as sensing.This can be very useful in applications like sensing. A polymer made from ethyl 2 - bromomethyl acrylate can be designed to specifically bind to a target molecule.A polymer made of ethyl 2-bromomethyl-acrylate can be specifically designed to bind to a molecule target. Once the binding occurs, the attached fluorescent dye can emit a signal, indicating the presence of the target.Once the binding has occurred, the fluorescent dye attached can emit a sign, indicating the target's presence.

In the pharmaceutical industry, this monomer can play a role in drug delivery systems.This monomer is used in the pharmaceutical industry to create drug delivery systems. Polymers synthesized from ethyl 2 - bromomethyl acrylate can be engineered to have controlled degradation properties.Polymers synthesized using ethyl 2-bromomethyl-acrylate can have controlled degradation properties. The bromomethyl groups can be used to conjugate drugs or targeting ligands to the polymer backbone.The bromomethyl group can be used to conjugate drug or targeting ligands with the polymer backbone. The resulting polymer - drug conjugate can then be designed to release the drug in a controlled manner, either in response to specific environmental conditions such as pH or enzymatic activity, or over a certain period of time.The polymer-drug conjugate can be designed to release a drug in a controlled way, either in response specific environmental conditions, such as pH, or enzymatic activities, or over a period of time.

Ethyl 2 - bromomethyl acrylate also has implications in the synthesis of specialty chemicals.Ethyl 2-bromomethyl-acrylate is also used in the synthesis specialty chemicals. It can serve as a building block in the synthesis of more complex organic compounds.It can be used as a building-block in the synthesis more complex organic compounds. The combination of the acrylate and bromomethyl groups allows for a series of sequential reactions.The combination of acrylate groups and bromomethyl group allows for a sequence of sequential reactions. For example, after the initial polymerization of the acrylate part, the bromomethyl groups can be used to link different polymer chains together, creating cross - linked polymers.After the initial polymerization, the bromomethyl group can be used to link together different polymer chains, creating cross-linked polymers. These cross - linked polymers often have enhanced mechanical and thermal properties compared to linear polymers.These cross-linked polymers have improved mechanical and thermal properties when compared to linear ones.

However, when working with ethyl 2 - bromomethyl acrylate, safety precautions must be taken.Safety precautions are required when working with ethyl 2-bromomethyl-acrylate. The bromine - containing compound can be toxic if ingested, inhaled, or if it comes into contact with the skin.Bromine-containing compounds can be toxic when ingested, if inhaled or if they come into contact with skin. It is also a reactive chemical, and proper handling procedures should be followed to prevent unwanted reactions.It is also a chemical that reacts, so it's important to follow the correct handling procedures to avoid unwanted reactions. In storage, it should be kept away from heat, light, and sources of ignition, as well as from reactive chemicals such as strong bases or reducing agents.It should be stored away from heat, sunlight, ignition sources, and reactive chemicals like strong bases or reducing agent.

In conclusion, ethyl 2 - bromomethyl acrylate is a monomer with great potential.Conclusion: ethyl 2-bromomethyl-acrylate is an acrylate monomer with a lot of potential. Its unique combination of an acrylate group for polymerization and a bromomethyl group for further functionalization makes it a valuable compound in materials science, pharmaceuticals, and specialty chemical synthesis.Its unique combination with an acrylate group to polymerize and a bromomethyl for further functionalization, makes it a valuable chemical compound in materials science and pharmaceuticals. By understanding its properties and reactivity, scientists can continue to develop new applications and improve existing processes that utilize this versatile monomer.Scientists can improve processes and develop new applications by understanding its properties and reactivity. As research progresses, we can expect to see even more innovative uses of ethyl 2 - bromomethyl acrylate in the future.We can expect to see more innovative uses for ethyl 2-bromomethyl-acrylate as research advances.