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Structure of 135908-33-7
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Methyl 4-aminobicyclo[2.2.2]octane-1-carboxylate features a rigid bicyclic scaffold that enforces conformational restraint, enhancing target selectivity in medicinal chemistry applications. The pendant amino group enables facile derivatization, while the ester functionality supports downstream transformations. This bench-stable compound integrates readily into complex molecular architectures.
Methyl 4-aminobicyclo[2.2.2]octane-1-carboxylate serves as a versatile scaffold for medicinal chemistry and asymmetric synthesis, offering a rigid, three-dimensional core with orthogonal functional handles. The pendant amine enables facile derivatization via acylation, alkylation, or reductive amination, while the ester group supports hydrolysis to the carboxylic acid or conversion to other carbonyl derivatives. Its bench-stable nature and compatibility with standard reaction conditions make it a practical building block for constructing complex heterocycles and bioactive molecules in drug discovery campaigns.
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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: