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Structure of 119844-67-6
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This chiral lactam features a rigid, electron-deficient ring system with a stereogenic center at the 5-position. The methyl group imparts steric bias, enhancing diastereoselectivity in asymmetric synthesis. Its bench-stable nature and compatibility with diverse reaction conditions make it a reliable scaffold for medicinal chemistry and natural product derivatization.
(5R)-5-Methylmorpholin-3-one serves as a stereochemically defined building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its constrained chiral scaffold enables selective transformations in asymmetric synthesis, while its lactam functionality offers predictable reactivity in nucleophilic additions and coupling reactions. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for scalable medicinal chemistry workflows.
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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: