Ethyl 3-amino-4,4,4-trifluorocrotonate CAS: 372-29-2
Catalog Number | XD93554 |
Product Name | Ethyl 3-amino-4,4,4-trifluorocrotonate |
CAS | 372-29-2 |
Molecular Formula | C6H8F3NO2 |
Molecular Weight | 183.13 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
Ethyl 3-amino-4,4,4-trifluorocrotonate is a compound that finds application in various areas including organic synthesis, medicinal chemistry, and material science.One major use of Ethyl 3-amino-4,4,4-trifluorocrotonate is as a building block in organic synthesis. It contains both an amine group and a double bond, which make it a versatile platform for creating more complex molecules. The amino group can be functionalized with various reagents to introduce a wide range of functionalities, while the double bond allows for further structural modifications. This compound is often employed in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds.In medicinal chemistry, Ethyl 3-amino-4,4,4-trifluorocrotonate has shown promising potential as a scaffold for the development of new drugs. The trifluoromethyl group is known to enhance the potency and metabolic stability of drugs, making it an attractive modification in drug design. This compound has been utilized in the synthesis of inhibitors targeting various enzymes and receptors, including kinases, proteases, and G protein-coupled receptors.Furthermore, Ethyl 3-amino-4,4,4-trifluorocrotonate also finds application in material science. Its unique trifluoromethyl group imparts desirable properties to the resulting materials, such as increased lipophilicity, improved electron-withdrawing ability, and altered molecular packing. This makes it useful in the development of functional materials, such as polymers, liquid crystals, and dyes.Additionally, Ethyl 3-amino-4,4,4-trifluorocrotonate can be used as a precursor in the synthesis of various fluorinated compounds. The trifluoromethyl group is an important moiety in many organic molecules due to its beneficial effects on physicochemical and biological properties. The compound can undergo various chemical transformations, such as nucleophilic substitution, oxidation, and reduction, to enable the introduction or modification of fluorinated groups.In summary, Ethyl 3-amino-4,4,4-trifluorocrotonate is a valuable compound with diverse applications in organic synthesis, medicinal chemistry, and material science. Its ability to serve as a building block, along with its unique trifluoromethyl group, makes it an essential component in the development of various pharmaceuticals, materials, and fluorinated compounds.