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Structure of 7480-32-2
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4-Phenyl-1,3-oxazolidin-2-one features a rigid oxazolidinone core with a phenyl substituent at the 4-position, conferring enhanced stability and defined stereochemical control. This scaffold integrates readily into chiral auxiliaries and serves as a key building block in asymmetric synthesis. The electron-withdrawing carbonyl group facilitates nucleophilic activation, enabling efficient transformations under mild conditions.
4-Phenyl-1,3-oxazolidin-2-one serves as a stable, bench-ready chiral building block for the synthesis of β-amino alcohols and oxazolidinone-containing pharmaceuticals. Its rigid five-membered ring structure enables selective nucleophilic ring-opening reactions with amines and thiols, facilitating access to diverse heterocyclic scaffolds under mild conditions. The phenyl substituent enhances solubility and provides orthogonal reactivity in multi-step syntheses.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: