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Structure of 1363380-79-3
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tert-Butyl 6-(aminomethyl)-2-azaspiro[3.3]heptane-2-carboxylate features a rigid spirocyclic core with a primary amine handle, enabling direct functionalization in medicinal chemistry. The tert-butyl ester group offers stability and convenient deprotection under mild acidic conditions. This scaffold integrates seamlessly into bioactive molecule design, particularly for constrained peptidomimetics and targeted kinase inhibitors.
tert-Butyl 6-(aminomethyl)-2-azaspiro[3.3]heptane-2-carboxylate serves as a versatile spirocyclic scaffold for medicinal chemistry and process development, enabling efficient access to constrained nitrogen-containing heterocycles. The protected amine and carboxylate functionalities offer orthogonal reactivity, facilitating sequential derivatization. Bench-stable and readily purified by standard chromatography, it functions as a key building block in the synthesis of bioactive molecules via amide coupling, reductive amination, or cyclization strategies.
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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: