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Structure of 55022-88-3
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1-Azabicyclo[2.2.2]octane-4-carboxylic acid is a rigid, nitrogen-containing bicyclic scaffold that integrates a carboxylic acid functional group at the bridgehead position. This structural motif imparts enhanced metabolic stability and defined spatial orientation, enabling precise molecular positioning in medicinal chemistry applications. The compound serves as a key building block for bioactive molecule synthesis, particularly in CNS-targeted drug discovery where conformational restraint improves target engagement.
1-Azabicyclo[2.2.2]octane-4-carboxylic acid serves as a rigid, conformationally constrained scaffold for medicinal chemistry applications. Its bicyclic structure imparts enhanced metabolic stability and defined spatial orientation, facilitating targeted interactions in drug design. The carboxylic acid group enables direct derivatization or salt formation, while the tertiary amine supports pH-dependent solubility and bioavailability modulation. This compound functions effectively in peptide mimetics, kinase inhibitors, and CNS-targeted lead optimization.
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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: