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Structure of 137280-49-0
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2,4,6-Trimethylbenzenesulfinamide features a sterically shielded sulfinamide group attached to a highly substituted aromatic ring. This configuration imparts exceptional stability and resistance to oxidation, enabling reliable use in asymmetric synthesis. The electron-rich aryl core enhances reactivity in transition-metal-catalyzed transformations. Its bench-stable nature simplifies handling in multi-step sequences.
2,4,6-Trimethylbenzenesulfinamide serves as a stable, bench-ready sulfinamide source for stereoselective synthesis of sulfimines and sulfoxides. Its electron-donating trimethylphenyl group enhances reactivity in asymmetric α-amination and C–H functionalization processes. The compound exhibits excellent functional group tolerance and facilitates straightforward purification, making it a practical choice for complex molecule assembly in 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: