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Structure of 1595319-97-3
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This chiral sulfinamide features a stereogenic center at the sulfinyl carbon and combines a diphenylphosphinoaryl group with a bulky tert-butyl substituent. The scaffold enables asymmetric induction in transition metal-catalyzed reactions, delivering high enantioselectivity in C–H functionalization and cross-coupling processes.
[S(R)]-N-[(S)-[2-(Diphenylphosphino)phenyl]phenylmethyl]-2-methyl-2-propanesulfinamide serves as a chiral auxiliary in asymmetric synthesis, enabling stereoselective transformations through its rigid, well-defined chiral environment. The sulfinamide moiety facilitates enantioselective α-alkylation and conjugate addition reactions, while the diphenylphosphino group provides orthogonal coordination for transition metal catalysis. Its bench-stable nature and compatibility with common purification methods make it a practical choice for complex molecule assembly.
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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+P364-P501
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Lot numbers can be found on the outside label of a product: