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Structure of 694439-03-7
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This bench-stable, moisture-tolerant heterocyclic scaffold features a rigid bicyclic core with a protected carboxylate group, enabling straightforward functionalization. The (4aR,7aS)-rel stereochemistry ensures high diastereoselectivity in downstream transformations, making it ideal for constructing complex nitrogen-containing architectures in medicinal chemistry and synthetic methodology.
(4aR,7aS)-rel-tert-Butyl tetrahydro-2H-[1,4]dioxino[2,3-c]pyrrole-6(3H)-carboxylate serves as a robust heterocyclic building block for medicinal chemistry campaigns, enabling efficient access to complex pyrrolidine-fused scaffolds. Its bench-stable tert-butyl ester facilitates straightforward deprotection and functionalization, while the fused dioxinopyrrole core exhibits favorable solubility and compatibility with standard coupling reactions. This compound functions effectively in multistep syntheses requiring stereocontrolled construction of nitrogen-containing ring systems.
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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: