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Structure of 104227-71-6
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This chiral carbamate features a bench-stable, moisture-tolerant tert-butyl group attached to a stereodefined tetrahydrofuran ring. The 5-oxo functionality enables selective transformations at the C5 position, while the carbamate handles nitrogen protection efficiently in asymmetric synthesis workflows.
(S)-tert-Butyl (5-oxotetrahydrofuran-3-yl)carbamate serves as a valuable chiral building block in synthetic organic chemistry, enabling stereoselective access to oxygen-containing heterocycles. The molecule features a stable, bench-ready carbamate-protected amine and a ketone functionality at C5, both of which participate reliably in standard transformations such as reductive amination, nucleophilic addition, and enolate chemistry. Its defined stereochemistry and compatibility with common reaction conditions make it well-suited for the construction of complex intermediates in medicinal chemistry and natural product synthesis.
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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: