4-Amino-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid, also known by its CAS number 142847-17-4, is an organic compound characterized by the presence of both amino and carbonyl functional groups, which contribute to its reactivity and potential applications in organic synthesis and medicinal chemistry. This compound features a tert-butoxycarbonyl (Boc) protecting group, commonly used to protect amines during chemical reactions, enhancing its stability and selectivity in various synthetic pathways. The structure includes a four-carbon backbone with a ketone and two amino groups, which can participate in various chemical reactions, including peptide synthesis and other coupling reactions. Its solubility in polar solvents and moderate stability under standard conditions make it a useful intermediate in the synthesis of more complex molecules. Additionally, the presence of the amino and carbonyl groups suggests potential biological activity, making it of interest in pharmaceutical research. Overall, this compound exemplifies the versatility of amino acids and their derivatives in synthetic organic chemistry.

4-amino-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid

142847-17-4: N~2~-(tert-butoxycarbonyl)asparagine, Boc-DL-asparagine

4-AMINO-2-[(TERT-BUTOXYCARBONYL)AMINO]-4-OXOBUTANOIC ACID

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CAS 142847-17-4: 4-amino-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid

4-AMINO-2-[(TERT-BUTOXYCARBONYL)AMINO]-4-OXOBUTANOIC ACID

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N2-[(1,1-Dimethylethoxy)Carbonyl]-Asparagine

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4-amino-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid

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