| 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.
