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Structure of 67706-68-7
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Ethyl 4-((tert-butoxycarbonyl)amino)-3-oxobutanoate features a masked α-amino ketone scaffold, enabling direct incorporation into peptide-like architectures. The tert-butoxycarbonyl group provides orthogonal protection for amine functionalities, while the β-keto ester moiety supports facile cyclization and C–C bond formation under mild conditions. This reagent streamlines access to complex heterocyclic frameworks in synthetic medicinal chemistry and natural product synthesis.
Ethyl 4-((tert-butoxycarbonyl)amino)-3-oxobutanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to β-amino carbonyl scaffolds. The molecule combines a stable tert-butyl carbamate (Boc) protecting group with an α,β-unsaturated ester motif, facilitating sequential transformations including reduction, alkylation, and cyclization. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for peptide-like fragment synthesis and heterocycle construction in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: