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Structure of 852212-90-9
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This sulfonamide features a chiral amine scaffold paired with a sterically hindered, electron-rich trimethylbenzenesulfonyl group. The diphenylethyl backbone imparts conformational rigidity, while the sulfonyl moiety enhances solubility and metabolic stability. Designed for asymmetric synthesis applications, it serves as a robust chiral auxiliary in enantioselective transformations.
N-((1R,2R)-2-Amino-1,2-diphenylethyl)-2,4,6-trimethylbenzenesulfonamide serves as a chiral sulfonamide auxiliary in asymmetric synthesis, enabling stereoselective transformations through its rigid diphenyl-substituted backbone and sterically shielded sulfonamide group. The ortho-methylated aryl sulfonamide enhances bench stability and facilitates purification, while the primary amine supports diverse functionalization pathways. It functions effectively in enantioselective derivatization and acts as a robust chiral scaffold for target-oriented synthesis.
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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: