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Structure of 6485-45-6
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rel-(2R,6R)-2,6-Dimethylmorpholine is a chiral, bench-stable heterocycle featuring two methyl groups at the 2- and 6-positions of the morpholine ring. This stereochemistry imparts distinct conformational rigidity and enhanced solubility in polar organic solvents. The compound serves as a tailored building block in asymmetric synthesis, particularly for constructing nitrogen-containing scaffolds with defined spatial orientation. Its stability under standard conditions facilitates handling in process development workflows.
rel-(2R,6R)-2,6-Dimethylmorpholine serves as a stereodefined, bench-stable heterocyclic building block for medicinal chemistry and catalysis. Its constrained conformation enhances rigidity in target molecules, improving binding selectivity. The tertiary amine functionality enables efficient salt formation and facilitates protonation in synthetic transformations. Exhibiting excellent functional group tolerance and compatibility with standard coupling reactions, it functions as a versatile scaffold in the synthesis of bioactive compounds and catalysts.
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GHS Pictogram :
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GHS No : GHS02,GHS05,GHS06
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Signal Word : Danger
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UN#: 1992
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Class : 3 (6.1)
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Packing Group : Ⅲ
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Hazard Statements : H226-H311-H318
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: