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Structure of 1212182-03-0
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tert-Butyl (R)-3-(2-hydroxyethyl)pyrrolidine-1-carboxylate features a chiral pyrrolidine core with a pendant hydroxyl group, enabling selective functionalization in asymmetric synthesis. The tert-butyl ester offers stability and ease of removal under mild acidic conditions. This scaffold integrates readily into bioactive molecule design, particularly in medicinal chemistry campaigns targeting CNS modulators and enzyme inhibitors.
tert-Butyl (R)-3-(2-hydroxyethyl)pyrrolidine-1-carboxylate serves as a chiral building block for the synthesis of bioactive heterocycles and medicinal intermediates. The pyrrolidine core provides a rigid, stereodefined scaffold with orthogonal functionality: the tert-butoxycarbonyl (Boc) group enables selective deprotection under mild acidic conditions, while the pendant hydroxyl moiety facilitates derivatization via etherification or esterification. This combination supports efficient route design in peptide-like compound development and offers bench-stable handling with good solubility in common organic solvents.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: