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Structure of 24601-74-9
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(S)-4-Isopropyloxazolidine-2,5-dione is a chiral synthon featuring a rigid oxazolidinone core that enables stereoselective transformations. This bench-stable derivative integrates seamlessly into asymmetric synthesis workflows, where its defined stereochemistry directs enantioselective bond formation. The isopropyl substituent enhances solubility and modulates reactivity, facilitating efficient coupling reactions under mild conditions.
(S)-4-Isopropyloxazolidine-2,5-dione serves as a chiral synthon for asymmetric synthesis, enabling stereoselective construction of β-amino acid derivatives and peptidomimetics. Its oxazolidinone core exhibits high bench stability, excellent functional group tolerance, and compatibility with standard coupling conditions. The molecule facilitates efficient enantioselective transformations via controlled ring-opening reactions, making it a practical building block for medicinal chemistry campaigns requiring defined stereochemistry.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: