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Structure of 1250997-29-5
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This azabicyclic scaffold integrates a tert-butoxycarbonyl-protected amine and a carboxylic acid handle, enabling direct incorporation into peptide macrocycles and constrained peptidomimetics. The rigid bicyclic core enhances conformational preorganization, while the orthogonal functional groups support sequential derivatization under standard coupling conditions.
3-(tert-Butoxycarbonyl)-3-azabicyclo[3.2.1]octane-8-carboxylic acid serves as a versatile scaffold for the synthesis of nitrogen-containing heterocycles, particularly in medicinal chemistry applications. The protected amine and carboxylic acid functionalities enable orthogonal transformations, while the bicyclic core provides conformational rigidity. Its bench-stable tert-butyl ester facilitates straightforward deprotection and derivatization, supporting efficient access to diverse analogs via standard coupling and reduction protocols.
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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: