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Structure of 870089-49-9
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tert-Butyl 3-acetylazetidine-1-carboxylate features a sterically hindered azetidine core with a strategically positioned acetyl group, enabling direct functionalization at the nitrogen. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences for medicinal chemistry and peptide derivatization. The tert-butyl ester facilitates selective deprotection under mild acidic conditions, streamlining access to functionalized azetidines.
tert-Butyl 3-acetylazetidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to azetidine-containing scaffolds. The acetyl group provides a handle for selective transformations, while the tert-butoxycarbonyl (Boc) protection ensures stability and ease of deprotection under mild acidic conditions. Its compatibility with standard coupling reactions and functional group tolerance makes it well-suited for iterative synthesis of complex heterocycles and API intermediates.
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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: