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Structure of 2253984-99-3
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This chiral sulfinamide scaffold features a sterically shielded di-tert-butylphosphanyl group and a rigid biphenyl framework, enabling high enantioselectivity in asymmetric synthesis. The bench-stable, moisture-tolerant structure integrates seamlessly into transition-metal-catalyzed transformations, offering robust stereocontrol in complex molecule assembly.
[S(R)]-N-[(1S)-1-[2-(Di-tert-butylphosphanyl)phenyl]phenylmethyl]-N,2-dimethyl-2-propanesulfinamide serves as a highly effective chiral auxiliary in asymmetric synthesis, enabling stereoselective C–C bond formation. Its robust di-tert-butylphosphanyl group enhances coordination stability with transition metals, while the sulfinamide moiety provides excellent stereocontrol and bench stability. The molecule facilitates efficient enantioselective transformations under standard catalytic conditions, offering predictable outcomes and straightforward purification—ideal for iterative synthetic sequences in medicinal chemistry and process development workflows.
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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: