| product_name | alpha-Trifluoromethylacrylic acid tert-butylester |
| CAS_number | 136529-75-4 |
| formula | C8H11F3O2 |
| molar_mass | 196.17 |
| density | Not specified |
| boiling_point | Not specified |
| melting_point | Not specified |
| appearance | Not specified |
| odor | Not specified |
| solubility | Not specified |
| refractive_index | Not specified |
| flash_point | Not specified |
| vapor_pressure | Not specified |
| thermal_stability | Not specified |
What is alpha-Trifluoromethylacrylic acid-tert-butylester?
Alpha-Trifluoromethylacrylic acid-tert-butylester is a compound that belongs to the family of acrylic acid esters. It is characterized by the presence of a trifluoromethyl group attached to the alpha position of the acrylic acid moiety, along with a tert-butyl ester group.
What are the key properties of alpha-Trifluoromethylacrylic acid-tert-butylester?
This compound is known for its high chemical stability, resistance to hydrolysis, and excellent solubility in organic solvents. It has a low melting point and boiling point, making it suitable for a wide range of applications.
What are the potential applications of alpha-Trifluoromethylacrylic acid-tert-butylester?
Alpha-Trifluoromethylacrylic acid-tert-butylester is commonly used as a building block in organic synthesis, especially in the pharmaceutical and agrochemical industries. It can be employed in the preparation of various functionalized molecules due to its unique structure and reactivity.
What are the advantages of using alpha-Trifluoromethylacrylic acid-tert-butylester in chemical synthesis?
One of the main advantages of using this compound is the presence of the trifluoromethyl group, which can impart desirable properties to the final products, such as increased lipophilicity and metabolic stability. Additionally, the tert-butyl ester group can serve as a protecting group or a precursor for further functionalization.
How is alpha-Trifluoromethylacrylic acid-tert-butylester synthesized?
Alpha-Trifluoromethylacrylic acid-tert-butylester can be synthesized through the reaction of trifluoromethyl acrylic acid with tert-butyl alcohol in the presence of a suitable catalyst. The reaction typically proceeds under mild conditions and yields the desired product in good to excellent yields.
What are some key considerations when handling alpha-Trifluoromethylacrylic acid-tert-butylester in the laboratory?
It is important to handle this compound with care due to its potential reactivity and toxicity. Proper personal protective equipment should be worn, and the compound should be stored in a well-ventilated area away from sources of ignition. Additionally, standard safety protocols for handling organic compounds should be followed.
Are there any recent developments or research studies involving alpha-Trifluoromethylacrylic acid-tert-butylester?
Recent studies have highlighted the utility of alpha-Trifluoromethylacrylic acid-tert-butylester in the development of novel drug candidates and bioactive molecules. Researchers have explored its use in medicinal chemistry, catalysis, and materials science, demonstrating its versatility and potential for future applications.
What sets alpha-Trifluoromethylacrylic acid-tert-butylester apart from other acrylic acid derivatives?
The unique trifluoromethyl group in alpha-Trifluoromethylacrylic acid-tert-butylester distinguishes it from other acrylic acid derivatives and imparts distinct chemical and physical properties. This feature opens up new possibilities for designing molecules with tailored functions and enhanced performance.
In summary, alpha-Trifluoromethylacrylic acid-tert-butylester is a versatile compound with a wide range of applications in organic synthesis, medicinal chemistry, and materials science. Its unique structure and properties make it a valuable building block for the development of novel molecules with desired functionalities and biological activities. Researchers and chemists continue to explore the potential of this compound in various fields, showcasing its importance in modern chemistry and drug discovery.