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Structure of 1824024-00-1
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This tert-butyl 6-(methylamino)-2-azaspiro[3.3]heptane-2-carboxylate features a spirocyclic core with a methylamino substituent, delivering enhanced rigidity and defined stereochemistry. The tert-butyl ester group enables convenient deprotection under mild acidic conditions, facilitating downstream functionalization. This scaffold serves as a valuable chiral building block in medicinal chemistry, particularly for targeted kinase inhibitors and CNS-active compounds.
tert-Butyl 6-(methylamino)-2-azaspiro[3.3]heptane-2-carboxylate serves as a versatile spirocyclic scaffold for medicinal chemistry, enabling efficient access to constrained nitrogen-containing heterocycles. The protected amine and carboxylate functionalities offer orthogonal reactivity, facilitating downstream derivatization via amide coupling or reductive amination. Bench-stable and readily purified by flash chromatography, it functions as a key building block in the synthesis of bioactive molecules with defined stereochemistry.
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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: