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Structure of 127926-24-3
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This azabicyclic scaffold features a tert-butoxycarbonyl-protected amine, enabling direct incorporation into peptide and small-molecule synthesis. The rigid bicyclic core imparts conformational stability, while the carboxylic acid functionality supports efficient coupling reactions under standard conditions.
2-[(tert-Butoxy)carbonyl]-2-azabicyclo[2.1.1]hexane-1-carboxylic acid serves as a versatile, bench-stable building block for the synthesis of constrained azabicyclic scaffolds. Its tert-butyl ester group enables straightforward deprotection under mild acidic conditions, while the bicyclic core provides defined stereochemistry and rigidity ideal for medicinal chemistry applications. The carboxylic acid functionality facilitates efficient coupling reactions, supporting diverse functionalization in peptide and small-molecule library development.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: