tert-butyl 2-amino-3-[(2-methylpropan-2-yl)oxy]propanoate
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This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure, featuring an amino group at the 2-position, a tert-butyl ester, and a tert-butoxy group (2-methylpropan-2-yl)oxy at the 3-position, makes it a protected derivative of serine, particularly useful in peptide synthesis and the development of pharmaceutical intermediates. The tert-butyl groups provide steric protection for both the carboxylic acid and the hydroxyl group, enhancing stability during reactions, while the amino group allows for further functionalization. It is often employed in the synthesis of bioactive compounds, including potential drug candidates, where its unique properties facilitate the creation of specific molecular architectures. Additionally, it can serve as a precursor in the production of specialty chemicals used in research and industrial applications.
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