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Structure of 928038-44-2
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3-Azetidinemethanol (hydrochloride) delivers a reactive azetidine core with a pendant hydroxymethyl group, enabling direct functionalization in medicinal chemistry. This bench-stable, moisture-tolerant scaffold integrates readily into target-oriented synthesis, offering enhanced solubility and metabolic stability for bioactive molecule design.
3-Azetidinemethanol (hydrochloride) serves as a versatile building block for the synthesis of bioactive heterocycles, particularly in medicinal chemistry applications. Its primary amine functionality enables straightforward derivatization, while the hydrochloride salt enhances stability and solubility for handling. The molecule functions effectively in nucleophilic substitution reactions and facilitates the construction of pyrrolidine-containing scaffolds via cyclization protocols. Its bench-stable nature and compatibility with standard coupling conditions make it well-suited for iterative synthesis workflows.
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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: