2-Bromoethyl acrylate
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- Molecular formula
- C5H7BrO2
- CAS Number
- 588-38-1
- IUPAC Name
- 2-bromoethyl prop-2-enoate
- Molecular Weight
- 180.01g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5040g/cm3
- Appearance
- can vary slightly due to impurities, but it generally retains a clear to slightly yellow hue when pure.
- Synonyms
- 2-BROMOETHYL ACRYLATE
Identification
Interesting facts
Interesting Facts about 2-bromoethyl prop-2-enoate
2-bromoethyl prop-2-enoate is a fascinating compound that holds significant value in the realm of organic chemistry. Here are some notable aspects that highlight its importance:
- Reactivity: As an alkyl halide, it can undergo various nucleophilic substitution reactions. This makes it a versatile building block for synthesizing more complex molecules.
- Ester Linkage: The presence of the ester functional group in its structure provides the compound with unique chemical properties, such as participating in transesterification reactions, which are vital in the production of biodiesel.
- Applications in Polymer Chemistry: 2-bromoethyl prop-2-enoate can serve as a monomer in the production of polymers. Its ability to undergo polymerization makes it a candidate for creating materials with specific properties, such as elasticity and strength.
- Biological Activity: Research suggests that derivatives of 2-bromoethyl prop-2-enoate may exhibit interesting biological properties, which could lead to potential applications in drug development.
- Synthesis: Scientists can synthesize this compound through various methods, including using alkylation reactions to introduce the bromo group, showcasing the principles of synthetic organic chemistry.
Studying 2-bromoethyl prop-2-enoate not only emphasizes the importance of functional groups in determining chemical behavior but also opens doors to innovative applications across various scientific fields. As chemists continue to explore its capabilities, the compound remains an intriguing subject of study.