Interesting facts
Interesting Facts about 2,2,2-Trifluoroethyl 2-Methylprop-2-enoate
2,2,2-Trifluoroethyl 2-methylprop-2-enoate is a fascinating compound that belongs to the category of *fluorinated olefins*. Its unique structure gives it some remarkable properties and applications:
- Fluorination Benefits: The presence of trifluoromethyl groups in its structure enhances the compound's stability and reactivity, making it valuable in synthetic chemistry.
- Applications: This compound is widely used in the formulation of specialty polymers, pharmaceuticals, and agrochemicals due to its ability to impart desirable chemical characteristics.
- Polymer Production: It can be polymerized to form copolymers that possess improved thermal and chemical resistance, which is crucial in creating materials for demanding industrial applications.
- Biological Activity: In medicinal chemistry, fluorinated compounds are often evaluated for their biological activity; the fluorine atoms can influence the interaction between the molecule and biological targets.
Interestingly, the synthesis of this compound showcases the *versatility of organofluorine chemistry*, where fluorine atoms replace hydrogen atoms in organic compounds to modify physical and chemical properties significantly. In the words of chemist Eric C. Trump:
“Fluorinated compounds are the unsung heroes of modern chemistry, paving the way for innovations in materials science and pharmaceuticals.”
In summary, 2,2,2-trifluoroethyl 2-methylprop-2-enoate is more than just a chemical entity; it embodies the excitement of creating new materials and serves as a platform for advancing various fields in science and technology.
Synonyms
2,2,2-TRIFLUOROETHYL METHACRYLATE
352-87-4
Trifluoroethyl methacrylate
2,2,2-trifluoroethyl 2-methylprop-2-enoate
2-Propenoic acid, 2-methyl-, trifluoroethyl ester
Methacrylic acid 2,2,2-trifluoroethyl ester
EINECS 206-525-3
NSC 32617
2-Propenoic acid, 2-methyl-, 2,2,2-trifluoroethyl ester
DTXSID7059856
Methacrylic acid, 2,2,2-trifluoroethyl ester
2,2,2-Trifluoroethyl Methacrylate (stabilized with MEHQ)
2,2,2-TRIFLUOROETHYLMETHACRYLATE
MFCD00013576
TFEMA
SCHEMBL36595
2-methyl-2-propenoic acid 2,2,2-trifluoroethyl ester
2,2-Trifluoroethyl methacrylate
DTXCID0038962
98% GC(stabilized with MEHQ)
2,2,2-trifluoroethyl-methacrylate
NSC32617
FD2010
MFCD00274739
NSC-32617
AKOS005063599
CS-W017819
AS-48910
FT104797
Methacrylic acid,2,2-trifluoroethyl ester
2,2,2-Trifluoroethyl 2-methylacrylate #
DB-048768
M0738
NS00020641
EN300-7692027
A822708
2,2,2-tris(fluoranyl)ethyl 2-methylprop-2-enoate
2,2,2-Trifluoroethyl Methacrylate, (stabilized with MEHQ)
2,2,2-Trifluoroethyl methacrylate, stab. w/ 100 ppm MEHQ
2,2,2-Trifluoroethyl methacrylate, contains 100 ppm MEHQ as stabilizer, 98%
2,2,2-Trifluoroethyl methacrylate, contains 50-200 ppm MEHQ as inhibitor, 99%
206-525-3
Solubility of 2,2,2-Trifluoroethyl 2-Methylprop-2-enoate
2,2,2-Trifluoroethyl 2-methylprop-2-enoate, with its unique structure that includes fluorinated groups, presents intriguing solubility characteristics. The presence of three fluorine atoms typically increases the polarity of the compound, influencing its interactions with solvents. Here are some key points to consider regarding its solubility:
In conclusion, while 2,2,2-trifluoroethyl 2-methylprop-2-enoate is likely to be soluble in various solvents due to its fluorinated nature, the exact solubility will depend significantly on the solvent environment and conditions. As with many fluorinated compounds, its solubility can be a fascinating feature worthy of further study.