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CAS 1528769-14-3

:

(2S)-2-Amino-4-methyl-1-((2S)-2-methyloxiranyl)-1-pentanone trifluoroacetate

Description:
(2S)-2-Amino-4-methyl-1-((2S)-2-methyloxiranyl)-1-pentanone trifluoroacetate is a chemical compound characterized by its specific stereochemistry and functional groups. It features an amino group, a ketone, and an epoxide, which contribute to its reactivity and potential biological activity. The presence of the trifluoroacetate moiety indicates that it is a salt form, which can enhance its solubility and stability in various solvents. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic attacks due to the electrophilic nature of the carbonyl group and the epoxide ring's strain. Its stereochemical configuration is crucial for its interaction with biological systems, potentially influencing its pharmacological properties. As with many amino acids and their derivatives, this compound may exhibit chiral properties, which can affect its behavior in biological contexts, such as enzyme interactions or receptor binding. Overall, the unique combination of functional groups and stereochemistry makes this compound of interest in medicinal chemistry and synthetic applications.
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