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Structure of 1807938-50-6
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This chiral morpholine derivative features a tert-butoxycarbonyl-protected amine and a carboxylic acid group, enabling direct incorporation into peptide synthesis. The (2R,3S) stereochemistry ensures high diastereoselectivity in coupling reactions, while the bench-stable, moisture-tolerant nature simplifies handling.
(2R,3S)-4-(tert-Butoxycarbonyl)-2-methylmorpholine-3-carboxylic acid serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of constrained peptidomimetics and heterocyclic scaffolds. Its well-defined stereochemistry and orthogonal functional groups facilitate efficient coupling reactions and selective transformations. The Boc group provides stability during synthesis and can be readily removed under mild acidic conditions, simplifying purification and downstream derivatization.
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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-H315-H319-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: