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Structure of 215917-98-9
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This chiral morpholine derivative features a tert-butyl group and a methyl substituent at the 4- and 3-positions, respectively, with the (S)-configuration at the 3-position. The dicarboxylate functionality enables efficient incorporation into synthetic scaffolds, particularly in medicinal chemistry applications requiring stereochemical control. Bench-stable and moisture-tolerant, it serves as a robust building block for complex heterocyclic systems.
4-(tert-Butyl)3-methyl(S)-morpholine-3,4-dicarboxylate serves as a stereochemically defined morpholine scaffold for medicinal chemistry campaigns, enabling direct incorporation into bioactive molecules via standard coupling protocols. The tert-butyl ester group provides bench stability and orthogonal deprotection under mild acidic conditions, while the methyl and carboxylate functionalities offer controlled reactivity for amide formation and further functionalization. Functions as a key building block in the synthesis of heterocyclic APIs and kinase inhibitors.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: