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Structure of 1980007-51-9
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This chiral spirocyclic scaffold features a protected amine and carboxylic acid, enabling direct incorporation into peptide-like architectures. The tert-butoxycarbonyl group ensures stability during synthesis, while the azaspiro framework imparts conformational rigidity ideal for medicinal chemistry applications.
(S)-6-(tert-Butoxycarbonyl)-6-azaspiro[3.4]octane-7-carboxylic acid serves as a stereocontrolled building block for spirocyclic scaffolds prevalent in medicinal chemistry. The protected amine and carboxylic acid functionalities enable sequential derivatization, including deprotection, coupling, and cyclization reactions. Its robust tert-butoxycarbonyl group offers excellent bench stability and compatibility with standard peptide synthesis protocols, facilitating efficient access to complex nitrogen-containing heterocycles.
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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: