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Structure of 154634-96-5
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(3S,5S)-3,5-Dimethylmorpholine is a chiral, bench-stable heterocycle featuring a saturated morpholine core with defined stereochemistry at the 3- and 5-positions. This configuration imparts distinct conformational rigidity and directional polarity, enabling selective engagement in asymmetric synthesis. The molecule integrates readily into catalytic systems and serves as a tailored ligand or auxiliary in stereoselective transformations.
(3S,5S)-3,5-Dimethylmorpholine serves as a stable, chiral heterocyclic building block with well-defined stereochemistry, enabling stereoselective synthesis in medicinal chemistry. Its tertiary amine functionality facilitates salt formation and enhances solubility, while the constrained ring structure supports efficient functionalization at C3 and C5 positions. The compound exhibits excellent bench stability and compatibility with standard coupling and reduction protocols, making it a practical scaffold for constructing bioactive molecules and evaluating stereochemical effects in lead optimization.
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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 : H225-H303-H311-H316-H318
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P361-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: