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Structure of 132682-23-6
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This oxazolidinone derivative features a chiral (4R) center and a hydroxymethyl group, enabling selective functionalization in asymmetric synthesis. The cyclic carbamate structure provides stability and compatibility with diverse reaction conditions, facilitating integration into complex molecular architectures.
(4R)-4-(Hydroxymethyl)-1,3-oxazolidin-2-one serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective transformations through its pendant hydroxyl and lactam functionalities. It functions as a protected amino alcohol equivalent, offering stability and compatibility with common coupling and reduction protocols. Its well-defined stereochemistry facilitates incorporation into complex heterocyclic systems and peptide-like scaffolds, supporting efficient synthesis of bioactive molecules.
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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: