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Structure of 887924-07-4
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N-[(1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide features a chiral diamine scaffold flanked by two methoxy-substituted phenyl groups, enabling precise stereocontrolled synthesis. The sulfonamide moiety delivers enhanced solubility and hydrogen-bonding capacity, facilitating integration into bioactive molecule architectures under standard conditions.
N-[(1S,2S)-2-Amino-1,2-bis(4-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide serves as a chiral auxiliary in asymmetric synthesis, leveraging its rigid binaphthyl-like scaffold and amine functionality to direct stereoselective transformations. The sulfonamide group enhances solubility and facilitates purification, while the methoxy-substituted aryl moieties contribute to stability and compatibility with standard coupling reactions. This compound functions effectively in enantioselective derivatization and transition-metal-catalyzed processes.
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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: