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Structure of 949023-16-9
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This oxazolidine derivative features a chiral scaffold with defined (4S,5R) stereochemistry, integrating a benzoyl group at C3, a 4-methoxyphenyl substituent at C2, and a phenyl moiety at C4. The carboxylic acid at C5 enables conjugation or derivatization, supporting its use in asymmetric synthesis and medicinal chemistry applications.
(4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid serves as a stereochemically defined chiral building block for the synthesis of oxazolidinone-containing pharmaceutical intermediates. Its well-defined stereocenters and orthogonal functional groups enable reliable derivatization in peptide coupling and asymmetric synthesis. The molecule exhibits bench stability and facilitates purification via standard chromatographic methods, making it suitable for scalable medicinal chemistry campaigns requiring controlled stereochemistry and functional group compatibility.
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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: