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Structure of 87791-58-0
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Benzyl 4-oxoazetidine-2-carboxylate features a strained azetidine ring with a carbonyl at the 4-position and a benzyl ester at C2, offering a reactive handle for synthetic transformations. This electron-deficient heterocycle integrates readily into peptide mimetics and bioactive scaffolds, enabling efficient access to constrained analogs under standard conditions.
Benzyl 4-oxoazetidine-2-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to strained azetidine scaffolds. Its ketone functionality facilitates nucleophilic addition and reductive amination, while the benzyl ester allows for straightforward deprotection under mild conditions. The compound exhibits good bench stability and functional group tolerance, making it well-suited for use in medicinal chemistry campaigns involving heterocyclic core construction and late-stage derivatization.
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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: