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Structure of 511534-44-4
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N-((1R,2R)-2-Amino-1,2-diphenylethyl)methanesulfonamide features a chiral diphenylethyl scaffold paired with a methanesulfonamide group, enabling precise stereocontrolled synthesis in medicinal chemistry. The amine functionality supports derivatization, while the sulfonamide enhances solubility and hydrogen bonding capacity. This compound serves as a key building block for bioactive molecules requiring defined spatial orientation.
N-((1R,2R)-2-Amino-1,2-diphenylethyl)methanesulfonamide serves as a chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations through its rigid, enantiopure scaffold. The methanesulfonamide group provides excellent stability and facilitates purification, while the diphenylmethyl backbone offers robust steric control. This compound functions effectively in amine alkylation, acylation, and metal-catalyzed coupling reactions, supporting scalable access to complex chiral intermediates.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P264-P271-P301+P330+P331-P363-P501
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Lot numbers can be found on the outside label of a product: