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Structure of 1107658-75-2
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tert-Butyl cis-3-Hydroxy-4-methylpyrrolidine-1-carboxylate delivers a stereodefined pyrrolidine scaffold with orthogonal functionality. The cis configuration ensures predictable conformational control, while the hydroxyl group enables downstream derivatization. This bench-stable building block integrates readily into complex heterocyclic architectures and supports efficient synthesis of bioactive molecules under standard conditions.
tert-Butyl cis-3-Hydroxy-4-methylpyrrolidine-1-carboxylate serves as a versatile chiral building block for the synthesis of bioactive heterocycles and medicinal chemistry intermediates. The cis-configured pyrrolidine core provides defined stereochemistry, while the tert-butyl carbamate offers orthogonal protection compatible with standard deprotection protocols. The 3-hydroxy and 4-methyl functionalities enable downstream functionalization via oxidation, substitution, or coupling reactions, facilitating access to complex scaffolds in drug discovery workflows.
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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: