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Structure of 141699-58-3
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1-Boc-3-Methanesulfonyloxyazetidine features a strained azetidine core functionalized with a Boc-protected amine and a methanesulfonyloxy leaving group. This combination enables direct nucleophilic substitution under mild conditions, facilitating efficient C–N bond formation in synthetic sequences. The bench-stable, moisture-tolerant nature supports reliable handling in process development workflows.
1-Boc-3-methanesulfonyloxyazetidine serves as a versatile azetidine-based building block for medicinal chemistry, enabling efficient access to bioactive heterocycles. The methanesulfonyloxy group facilitates reliable nucleophilic substitution reactions under mild conditions, while the Boc protection ensures stability and compatibility with diverse reaction environments. Its bench-stable nature and predictable reactivity support straightforward functionalization and purification in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: