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Structure of 219823-47-9
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(R)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate serves as a chiral auxiliary in asymmetric synthesis, leveraging its stereodefined tetrahydrofuran core and stable sulfonate leaving group. This configurationally stable derivative facilitates stereoselective transformations under mild conditions, enabling efficient construction of enantiomerically enriched building blocks for medicinal chemistry applications.
(R)-Tetrahydrofuran-3-yl 4-methylbenzenesulfonate serves as a robust chiral auxiliary for stereoselective synthesis, enabling efficient C–O bond formation under mild conditions. Its bench-stable nature and excellent functional group tolerance facilitate reliable use in nucleophilic substitution reactions, particularly in the construction of enantiopure tetrahydrofuran derivatives. The tosyl leaving group provides high reactivity in SN2 processes, making it ideal for accessing complex heterocyclic scaffolds in medicinal chemistry 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-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: