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Structure of 103723-70-2
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This oxazolidinone scaffold features a branched isopropyl group at the 4-position, enhancing steric shielding and stability. The cyclic amide structure provides robustness under standard bench conditions, enabling reliable use in asymmetric synthesis and chiral auxiliaries.
4-(Propan-2-yl)-1,3-oxazolidin-2-one serves as a stable, bench-ready chiral building block for the synthesis of β-amino alcohols and heterocyclic scaffolds. Its oxazolidinone core enables efficient enantioselective transformations via ring-opening reactions with nucleophiles, offering high functional group tolerance and straightforward purification. This compound functions as a versatile auxiliary in asymmetric synthesis and is compatible with standard coupling protocols used in medicinal chemistry and process development.
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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-H320-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: