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Structure of 1626394-43-1
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This chiral bicyclic ester features a stereochemically defined ethyl 3-aminobicyclo[2.2.2]octane-2-carboxylate scaffold stabilized as the hydrochloride salt. The rigid, fused-ring architecture imparts conformational constraint ideal for asymmetric synthesis and medicinal chemistry applications. The amine functionality enables facile derivatization while the salt form enhances solubility and handling under standard bench conditions.
(2S,3S)-Ethyl 3-aminobicyclo[2.2.2]octane-2-carboxylate hydrochloride serves as a stereochemically defined, bench-stable building block for the synthesis of complex nitrogen-containing scaffolds. Its constrained bicyclic core and protected amine functionality enable selective functionalization in medicinal chemistry campaigns. The hydrochloride salt enhances solubility and stability, facilitating purification and use in standard coupling reactions, reductive amination, and heterocycle formation.
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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: