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Structure of 105258-93-3
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Benzyl 3-oxoazetidine-1-carboxylate features a strained azetidine ring bearing a carbonyl group at the 3-position, enabling direct functionalization in synthetic sequences. The benzyl ester facilitates convenient deprotection under standard conditions. This scaffold integrates readily into complex molecular architectures requiring controlled reactivity and spatial constraints.
Benzyl 3-oxoazetidine-1-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 offers convenient protection and orthogonal deprotection. The compound exhibits good bench stability and compatibility with diverse reaction conditions, making it well-suited for iterative synthesis of bioactive heterocycles and medicinal chemistry libraries.
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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: