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Structure of 2306261-01-6
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This spirocyclic amino acid derivative features a protected tertiary amine within a rigid 3.5-spirocycle framework, enabling controlled incorporation into peptide-based scaffolds. The tert-butoxycarbonyl group provides orthogonal protection for nitrogen functionalization, while the acetic acid side chain offers a handle for conjugation or further derivatization under standard coupling conditions.
2-(2-(tert-Butoxycarbonyl)-2-azaspiro[3.5]nonan-7-yl)acetic acid serves as a versatile spirocyclic building block for medicinal chemistry and peptide synthesis, enabling the incorporation of constrained azaspiro[3.5]nonane motifs into bioactive molecules. The tert-butyl carbamate group provides excellent stability and orthogonal protection, facilitating selective deprotection during downstream functionalization. Its acetic acid side chain allows for conjugation via amide or ester linkages, supporting applications in scaffold diversification and target-oriented 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: