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Structure of 191348-04-6
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This chiral pyrrolidine derivative features a formyl group at the 3-position and a tert-butyl carbamate protecting group, enabling direct functionalization in asymmetric synthesis. The bench-stable, moisture-tolerant scaffold facilitates efficient access to bioactive nitrogen heterocycles through reductive amination or nucleophilic addition protocols.
(S)-tert-Butyl 3-formylpyrrolidine-1-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to nitrogen-containing heterocycles. The aldehyde group facilitates standard transformations such as reductive amination, Wittig reactions, and nucleophilic additions, while the protected pyrrolidine scaffold offers excellent functional group tolerance and bench stability. Its well-defined stereochemistry supports asymmetric synthesis workflows, and the tert-butyl carbamate handle simplifies purification and downstream deprotection, making it ideal for iterative library construction and API precursor development.
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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: