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Structure of 134071-44-6
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This imidazole-containing dioxolane derivative features a sterically hindered, bench-stable scaffold with enhanced solubility in polar organic media. The para-methylbenzenesulfonate group enables efficient coupling reactions under mild conditions, while the cis-configuration ensures predictable stereochemical control in asymmetric synthesis workflows.
(cis-2-((1H-Imidazol-1-yl)methyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl)methyl 4-methylbenzenesulfonate serves as a stable, bench-ready glycosyl donor for stereoselective glycosylation reactions. The imidazole-bearing dioxolane scaffold enables efficient C-glycosylation under mild conditions, with the tosylate group facilitating activation via SN2 displacement. Its functional group tolerance and predictable stereocontrol make it a practical tool for constructing complex carbohydrate architectures and 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: