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Structure of 134676-67-8
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4-(tert-Butoxycarbonyl)thiomorpholine-2-carboxylic acid features a protected thiomorpholine-2-carboxylic acid scaffold with a robust tert-butoxycarbonyl group, enabling stable incorporation into peptide synthesis. The electron-deficient sulfur atom enhances reactivity in coupling reactions, while the steric bulk of the tert-butyl moiety minimizes side reactions. This derivative facilitates efficient access to bioactive thiomorpholine-containing compounds under standard conditions.
4-(tert-Butoxycarbonyl)thiomorpholine-2-carboxylic acid serves as a stable, bench-ready building block for the synthesis of thiomorpholine-based heterocycles. The Boc-protected carboxylic acid functionality enables straightforward deprotection and coupling reactions, facilitating access to diverse pharmaceutical scaffolds. Its functional group tolerance supports integration into multi-step synthetic sequences, particularly in medicinal chemistry campaigns targeting kinase inhibitors and other bioactive molecules.
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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: