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Structure of 868689-63-8
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This bench-stable, moisture-tolerant building block features a protected morpholine ring with a carboxylic acid handle. The tert-butoxycarbonyl group enables selective deprotection during peptide synthesis, while the electron-rich heterocycle supports diverse coupling reactions under standard conditions.
(S)-4-(tert-Butoxycarbonyl)morpholine-2-carboxylic acid serves as a key chiral building block for the synthesis of morpholine-containing peptidomimetics and bioactive heterocycles. The protected amine and carboxylic acid functionalities enable orthogonal transformations in solid-phase and solution-phase peptide coupling. Its bench-stable tert-butyl carbamate group facilitates selective deprotection under mild acidic conditions, while the morpholine core provides structural rigidity and hydrogen-bonding capacity relevant to drug-like scaffolds.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-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: