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Structure of 184346-45-0
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(S)-4-Isopropyl-5,5-diphenyloxazolidin-2-one is a chiral oxazolidinone scaffold featuring a sterically encumbered diphenyl-substituted ring and an isopropyl group at the 4-position. This configuration imparts high enantioselectivity in asymmetric synthesis, particularly in nucleophilic additions and catalytic transformations. The bench-stable, moisture-tolerant structure facilitates handling under standard conditions.
(S)-4-Isopropyl-5,5-diphenyloxazolidin-2-one serves as a robust chiral auxiliary in asymmetric synthesis, enabling high diastereoselective transformations through well-established enolate chemistry. Its bench-stable oxazolidinone core offers excellent functional group tolerance and facilitates stereoselective C–C bond formation, particularly in aldol and alkylation reactions. The diphenyl substitution enhances rigidity and stereocontrol, while the isopropyl group improves solubility and purification efficiency. Widely employed in medicinal chemistry workflows, it functions as a reliable scaffold for constructing complex chiral intermediates with predictable stereochemical outcomes.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: