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Structure of 915095-94-2
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This chiral tetrahydrofuran derivative features a 4-(2-chloro-5-iodobenzyl)phenoxy moiety that confers enhanced lipophilicity and metabolic stability. The (S)-configuration ensures high stereoselectivity in downstream synthetic transformations, making it a valuable scaffold for medicinal chemistry campaigns targeting CNS disorders and kinase inhibitors.
(S)-3-(4-(2-Chloro-5-iodobenzyl)phenoxy)tetrahydrofuran serves as a versatile building block for the synthesis of bioactive molecules, leveraging the iodine handle for palladium-catalyzed cross-coupling reactions. The tetrahydrofuran ring provides stereochemical control and structural rigidity, while the phenoxy linkage offers a robust scaffold for further functionalization. Its bench-stable nature and compatibility with standard coupling protocols make it suitable for medicinal chemistry and process development 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: