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Structure of 1239320-11-6
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tert-Butyl 6-((methylsulfonyl)oxy)-2-azaspiro[3.3]heptane-2-carboxylate features a spirocyclic azabicyclic core with a methylsulfonyl ether handle, enabling selective transformations in complex molecular scaffolds. The tert-butyl ester group provides stability and convenient deprotection under mild acidic conditions, while the sulfonyloxy moiety serves as an effective leaving group in nucleophilic substitution reactions. This compound integrates seamlessly into medicinal chemistry campaigns requiring robust, stereochemically defined building blocks.
tert-Butyl 6-((methylsulfonyl)oxy)-2-azaspiro[3.3]heptane-2-carboxylate serves as a versatile spirocyclic building block for medicinal chemistry, enabling efficient access to constrained azaspiro[3.3]heptane scaffolds. The methylsulfonyloxy group facilitates nucleophilic substitution under mild conditions, while the tert-butyl ester provides stability and convenient deprotection. Its functional group tolerance supports downstream transformations in complex molecule synthesis.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: