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Structure of 1211526-53-2
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This spirocyclic diacid derivative features a protected amine and carboxylic acid group, enabling direct incorporation into peptide synthesis. The tert-butoxycarbonyl moiety ensures stability during handling and reaction sequences. The rigid spirocyclic core provides defined stereochemistry and conformational control.
2-(tert-Butoxycarbonyl)-2-azaspiro[3.3]heptane-6-carboxylic acid serves as a versatile spirocyclic building block for the synthesis of nitrogen-containing heterocycles. The Boc-protected amine and carboxylic acid functionalities enable orthogonal functionalization, facilitating efficient peptide coupling and reductive amination workflows. Its rigid spirocyclic core enhances conformational control in medicinal chemistry applications, while the tert-butyl carbamate group offers excellent bench stability and ease of removal under mild acidic conditions.
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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: