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Structure of 104266-90-2
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(S)-4-Benzyl-3-(3-methylbutanoyl)oxazolidin-2-one is a chiral oxazolidinone scaffold featuring a benzylic stereocenter and a sterically hindered acyl group. This configuration enables high diastereoselective transformations in asymmetric synthesis, particularly in enantioselective C–H functionalization and conjugate addition reactions. The molecule exhibits bench-stable handling characteristics under standard conditions.
(S)-4-Benzyl-3-(3-methylbutanoyl)oxazolidin-2-one serves as a versatile chiral building block in asymmetric synthesis, enabling efficient access to β-amino acid derivatives and peptidomimetics. Its oxazolidinone core provides excellent stereocontrol in nucleophilic ring-opening reactions, while the benzyl and isovaleryl side chains offer orthogonal functional handles for further diversification. Bench-stable and readily purified by chromatography, it functions reliably in standard peptide coupling and cascade reaction protocols.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: