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Structure of 186202-57-3
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tert-Butyl N-[(2R)-morpholin-2-ylmethyl]carbamate features a chiral morpholinomethyl group that enables stereoselective transformations in peptide synthesis. This bench-stable carbamate delivers precise nitrogen protection with orthogonal deprotection compatibility, facilitating efficient coupling sequences under mild conditions.
tert-Butyl N-[(2R)-morpholin-2-ylmethyl]carbamate serves as a stable, bench-ready chiral building block for medicinal chemistry applications. It functions as a protected amine surrogate, enabling straightforward incorporation of the (2R)-morpholin-2-ylmethyl group into complex scaffolds. The tert-butyl carbamate moiety provides excellent stability and orthogonal deprotection compatibility, while the morpholine ring offers favorable solubility and metabolic stability in downstream compounds. Its defined stereochemistry ensures consistent reactivity in asymmetric synthesis.
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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: