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Structure of 1016731-24-0
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Benzyl 3-(aminomethyl)azetidine-1-carboxylate features a strained azetidine core with a pendant aminomethyl group, enabling direct functionalization. This bench-stable, moisture-tolerant reagent integrates readily into peptide-like scaffolds and serves as a key building block for bioactive molecule synthesis.
Benzyl 3-(aminomethyl)azetidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to azetidine-containing scaffolds. The benzyloxycarbonyl (Cbz) group provides stable protection of the primary amine, facilitating orthogonal functionalization and simplifying purification. Its aminomethyl side chain undergoes standard transformations—such as alkylation, acylation, and reductive amination—while maintaining compatibility with diverse coupling reactions and heterocycle formation protocols common in API development.
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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: