Ethyl {2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl}acetate is a chemical compound characterized by its thiazole and trifluoromethyl functionalities. The thiazole ring contributes to its heterocyclic nature, which often imparts unique reactivity and biological activity. The presence of the trifluoromethyl group enhances lipophilicity and can influence the compound's pharmacokinetic properties, making it potentially useful in medicinal chemistry. Ethyl acetate serves as an ester functional group, which can affect solubility and volatility. This compound may exhibit various properties such as moderate to high stability under standard conditions, and it may be soluble in organic solvents while having limited solubility in water. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as a synthetic intermediate in organic synthesis. As with many thiazole derivatives, it may also possess biological activity, warranting further investigation into its potential uses in drug development or as a biochemical probe. Safety and handling precautions should be observed due to the presence of fluorinated groups, which can pose environmental and health risks.

ethyl {2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl}acetate

680215-92-3: Ethyl {2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl}acetate is a chemical compound characterized by its thiazole and trifluoromethyl functionalities. The thiazole ring contributes to its heterocyclic nature, which often imparts unique reactivity and biological activity. The presence of the trifluoromethyl group enhances lipophilicity and can influence the compound's pharmacokinetic properties, making it potentially useful in medicinal chemistry. Ethyl acetate serves as an ester functional group, which can affect solubility and volatility. This compound may exhibit various properties such as moderate to high stability under standard conditions, and it may be soluble in organic solvents while having limited solubility in water. Its structure suggests potential applications in pharmaceuticals, agrochemicals, or as a synthetic intermediate in organic synthesis. As with many thiazole derivatives, it may also possess biological activity, warranting further investigation into its potential uses in drug development or as a biochemical probe. Safety and handling precautions should be observed due to the presence of fluorinated groups, which can pose environmental and health risks.

Ethyl 2-{2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl}acetate

CAS 680215-92-3

ethyl {2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl}acetate

Ethyl 2-{2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-4-yl}acetate

Ref: 54-PC32561