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Structure of 790184-33-7
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(2R)-2-Methylmorpholine is a chiral, bench-stable heterocycle featuring a stereogenic center at the 2-position. This configuration imparts distinct spatial orientation to the nitrogen lone pair, enhancing its utility in asymmetric synthesis and as a selective ligand in transition metal catalysis. The molecule’s polar, saturated ring structure enables favorable solubility in common organic solvents while maintaining low nucleophilicity under standard reaction conditions.
(2R)-2-Methylmorpholine serves as a chiral auxiliary and versatile building block in asymmetric synthesis, enabling stereoselective transformations through its well-defined stereochemistry. It functions effectively as a nucleophilic catalyst or ligand in transition-metal-catalyzed reactions, offering enhanced control in C–C and C–heteroatom bond formation. The compound exhibits favorable bench stability, ease of handling, and compatibility with common functional groups, making it a practical choice for iterative synthetic sequences and process-scale applications.
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GHS Pictogram :
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GHS No : GHS02,GHS05
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Signal Word : Danger
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UN#: 2920
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Class : 8 (3)
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Packing Group : Ⅱ
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Hazard Statements : H226-H314-H318
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Precautionary Statements : P210-P240-P241-P280-P370+P378
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Lot numbers can be found on the outside label of a product: