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Structure of 1257856-31-7
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tert-Butyl (S)-2-cyanomorpholine-4-carboxylate features a chiral morpholine core with a cyano group at the 2-position and a tert-butyl ester at the 4-position. This configuration enables direct incorporation into asymmetric synthesis workflows, where the electron-deficient cyano moiety facilitates nucleophilic addition and the bench-stable ester supports controlled deprotection under mild conditions.
tert-Butyl (S)-2-cyanomorpholine-4-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive heterocycles, enabling efficient access to morpholine-based scaffolds via cyanide hydrolysis or nucleophilic addition. Its tert-butyl ester group offers bench stability and facile removal under mild acidic conditions, while the (S)-configuration ensures enantioselective downstream transformations. Functions effectively in coupling reactions and serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and CNS therapeutics.
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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 : P261-P280-P304+P340
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Lot numbers can be found on the outside label of a product: