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Structure of 610794-20-2
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This chiral amino acid derivative features a prop-2-yn-1-yloxy-substituted phenyl group at the 4-position, enabling efficient copper-catalyzed coupling reactions. The alkyne handle facilitates click chemistry applications, while the (S)-configuration ensures stereochemical fidelity in peptide synthesis and bioconjugation workflows.
(S)-2-Amino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive heterocycles and peptidomimetics. The propargyloxy group enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating rapid access to triazole-linked scaffolds. Its bench-stable alkyne functionality, combined with orthogonal reactivity and well-defined stereochemistry, supports modular synthesis workflows in medicinal chemistry and process development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: