Interesting facts
Interesting Facts about 2-Chloroethyl 2-Methylprop-2-Enoate
2-Chloroethyl 2-methylprop-2-enoate is a fascinating compound that plays an important role in the field of organic chemistry and material science. This compound, also known for its reactivity, has several interesting traits:
- Versatile Reactivity: The presence of both a chlorine atom and an alkene group in its structure makes 2-chloroethyl 2-methylprop-2-enoate a highly reactive species. It can participate in various chemical reactions, such as nucleophilic substitutions and polymerizations.
- Applications in Synthesis: This compound serves as an excellent intermediate in organic synthesis. It can be used to generate a variety of useful compounds, including pharmaceuticals and agrochemicals.
- Importance in Polymer Chemistry: The unsaturated bond in the compound allows it to act as a monomer in polymerization reactions, leading to the creation of new materials with tailored properties.
- Biological Activity: Some derivatives of this compound may exhibit interesting biological properties, making it a topic of interest for drug development and medicinal chemistry.
As a scientist, exploring compounds like 2-chloroethyl 2-methylprop-2-enoate unveils a world rich in potential and innovation. Its unique structure and reactivity open doors to new possibilities in various fields:
- Medicinal Chemistry: Investigating its derivatives for therapeutic potential.
- Materials Science: Leveraging its chemical behavior to engineer novel synthetic materials.
- Environmental Applications: Exploring its role in developing eco-friendly pesticides.
In conclusion, 2-chloroethyl 2-methylprop-2-enoate embodies the wonders of chemistry, illustrating how a single compound can impact numerous scientific disciplines. As the saying goes, "Chemistry is a way of thinking about the world around us." This compound is a perfect example of that philosophy in action.
Synonyms
2-Chloroethyl methacrylate
2-Propenoic acid, 2-methyl-, 2-chloroethyl ester
.beta.-Chloroethyl methacrylate
EINECS 217-566-1
BRN 0956599
DTXSID6062042
3-02-00-01285 (Beilstein Handbook Reference)
beta-Chloroethyl methacrylate
DTXCID9035965
217-566-1
gpogmjlhwqhegf-uhfffaoysa-n
1888-94-4
2-chloroethyl 2-methylprop-2-enoate
Chloroethyl methacrylate
METHACRYLIC ACID, 2-CHLOROETHYL ESTER
NSC 18595
Methacrylic acid 2-chloroethyl ester
Z2YK45T5J9
NSC-18595
Methacrylic acid .beta.-chloroethyl ester
Methacrylic acid beta-chloroethyl ester
MFCD00045291
chloroethylmethacrylate
2-Chloroethylmethacrylate
UNII-Z2YK45T5J9
SCHEMBL112379
2-Chloroethyl 2-methylacrylate #
NSC18595
AKOS006229796
AS-67714
DB-044688
NS00026183
E83858
2-Chloroethyl methacrylate, stab. with 500ppm hydroquinone
2-Chloroethyl methacrylate, stab. with 400-600ppm hydroquinone
Solubility of 2-chloroethyl 2-methylprop-2-enoate
2-chloroethyl 2-methylprop-2-enoate, a compound with a unique structure, exhibits notable properties when it comes to its solubility. Understanding the solubility of this compound is essential for its applications in various chemical processes.
In summary, while 2-chloroethyl 2-methylprop-2-enoate is soluble in various organic solvents, it remains relatively insoluble in water. This property is crucial for chemists and researchers to consider when planning experiments or industrial applications involving this compound.