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Structure of 82961-77-1
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Methyl 4-(((benzyloxy)carbonyl)amino)-3-oxobutanoate features a protected α-amino ketone scaffold ideal for peptide synthesis and heterocyclic derivatization. The benzyl ester group ensures stability under standard conditions, while the keto functionality enables facile condensation reactions. This compound integrates seamlessly into complex molecular architectures with predictable reactivity.
Methyl 4-(((benzyloxy)carbonyl)amino)-3-oxobutanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to β-amino carbonyl frameworks. Its α,β-unsaturated ester functionality facilitates Michael additions and condensation reactions, while the benzyl carbamate group provides orthogonal protection for amine intermediates. The compound exhibits good bench stability and simplifies purification in multi-step syntheses, making it valuable for constructing heterocyclic scaffolds and peptide-derived motifs.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: