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Structure of 854250-89-8
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(r)-2-((Tert-butoxycarbonyl)amino)-3,3-dimethylpent-4-enoic acid features a sterically hindered, bench-stable α,β-unsaturated carbonyl system paired with a protected amine. This configuration enables direct incorporation into peptide synthesis workflows and facilitates downstream deprotection under mild acidic conditions. The molecule’s conjugated enoate moiety supports efficient coupling reactions while maintaining stability during storage and handling.
(r)-2-((Tert-butoxycarbonyl)amino)-3,3-dimethylpent-4-enoic acid serves as a versatile chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The protected amine and terminal alkyne functionalities enable efficient coupling reactions and downstream transformations, including palladium-catalyzed cross-couplings and cyclizations. Its tert-butyl carbamate group provides excellent stability and ease of purification, while the (r)-configuration ensures stereochemical fidelity in complex molecule assembly.
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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: