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Structure of 42267-27-6
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This chiral amide features a trifluoromethyl group and a reactive oxazolidinone ring, enabling selective conjugation in synthetic workflows. The (S)-configured scaffold supports stereocontrolled transformations, while the bench-stable, moisture-tolerant structure simplifies handling in complex synthesis.
(S)-N-(4-(2,5-Dioxooxazolidin-4-yl)butyl)-2,2,2-trifluoroacetamide serves as a versatile chiral building block for the synthesis of bioactive molecules, leveraging the oxazolidinone ring’s established role in asymmetric synthesis. Its trifluoroacetyl group enhances electrophilicity and provides a robust handle for selective transformations. The molecule exhibits excellent bench stability and facilitates efficient purification, making it well-suited for iterative synthetic sequences 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-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: