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*For research and further manufacturing use only, not for direct human use.
Structure of 90319-52-1
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Used for -amino acid synthesis and the preparation of -lactam antibiotics.
(R)-4-Phenyloxazolidin-2-one serves as a robust chiral auxiliary in asymmetric synthesis, enabling stereoselective enolate alkylations and aldol reactions. Its bench-stable nature and high diastereoselectivity facilitate efficient construction of complex α-hydroxy and α-amino acid derivatives. The oxazolidinone ring functions as a reliable directing group in transition-metal-catalyzed transformations and supports orthogonal protection strategies in peptide and natural product synthesis.
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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: