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Structure of 247089-85-6
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(R)-(-)-p-Toluenesulfinamide serves as a chiral auxiliary for asymmetric synthesis, enabling stereoselective α-amination of carbonyl compounds via imine formation. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to enantioenriched amines. The sulfinamide group provides excellent stereocontrol in Mannich-type reactions and functions as a removable directing group in catalytic transformations.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: