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Structure of 869681-70-9
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(R)-4-(tert-butoxycarbonyl)morpholine-3-carboxylic acid features a stereodefined morpholine core with a bench-stable tert-butyl ester protecting group, enabling straightforward functionalization in peptide synthesis and medicinal chemistry. The carboxylic acid moiety facilitates coupling reactions under standard conditions, while the cyclic amine scaffold provides conformational rigidity for targeted bioactive molecule design.
(R)-4-(tert-butoxycarbonyl)morpholine-3-carboxylic acid serves as a versatile chiral building block for the synthesis of bioactive heterocycles and peptide mimetics. The Boc-protected morpholine-3-carboxylic acid moiety offers excellent bench stability, compatibility with standard coupling conditions, and facilitates orthogonal deprotection during multi-step syntheses. Its defined stereochemistry enables reliable access to enantioselective scaffolds relevant to medicinal chemistry campaigns.
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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 : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: