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Structure of 91188-13-5
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tert-Butyl azetidin-3-ylcarbamate delivers a protected azetidine scaffold with enhanced stability and solubility, ideal for late-stage functionalization in medicinal chemistry. The tert-butyl carbamate group enables efficient deprotection under mild acidic conditions, while the strained azetidine ring imparts favorable conformational rigidity and metabolic resistance. This combination supports rapid access to bioactive nitrogen heterocycles in drug discovery workflows.
tert-Butyl azetidin-3-ylcarbamate serves as a stable, bench-ready building block for the synthesis of bioactive azetidine-containing compounds. Its carbamate group provides excellent functional group tolerance and facilitates straightforward deprotection under mild acidic conditions. The molecule enables efficient incorporation of the azetidin-3-yl scaffold into medicinal chemistry libraries and complex heterocyclic systems, particularly in late-stage diversification via nucleophilic substitution or transition-metal-catalyzed coupling reactions.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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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: