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Structure of 189321-66-2
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N-Boc-Morpholine-2-carboxylic acid features a morpholine ring bearing a Boc-protected carboxylic acid at the 2-position, enabling stable incorporation into peptide and small-molecule syntheses. The protected functionality facilitates selective deprotection under mild acidic conditions, streamlining access to bioactive intermediates. This bench-stable derivative supports efficient coupling reactions in diverse chemical contexts.
N-Boc-Morpholine-2-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of morpholine-containing scaffolds via standard deprotection and coupling protocols. Its Boc group provides excellent bench stability and orthogonal handling in multi-step syntheses, while the carboxylic acid functionality facilitates efficient amide bond formation under common coupling conditions. This compound functions reliably in peptide and heterocyclic library construction, offering predictable reactivity and straightforward purification.
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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: