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Structure of 2565792-23-4
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This chiral sulfinamide ligand features a sterically encumbered di-tert-butylphosphanyl group and a bulky isopropyl-substituted sulfonamide framework, enabling high enantioselectivity in asymmetric catalysis. The rigid scaffold facilitates precise substrate orientation, delivering exceptional stereocontrol in transition-metal-catalyzed transformations under standard conditions.
[S(R)]-N-[(1S)-1-[2-(Di-tert-butylphosphanyl)phenyl]phenylmethyl]-2-methyl-2-propanesulfinamide serves as a chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations via its robust sulfinamide group and sterically encumbered di-tert-butylphosphanyl moiety. Its bench-stable nature and compatibility with common reaction conditions facilitate efficient enantioselective C–C bond formation, particularly in the construction of α-amino acid derivatives and chiral building blocks for medicinal chemistry applications.
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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-H413
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Precautionary Statements : P264-P273-P280-P302+P352-P362-P501
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Lot numbers can be found on the outside label of a product: