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Structure of 205445-56-3
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This chiral building block features a protected amino group and a para-cyano-substituted phenyl moiety, enabling direct incorporation into peptide architectures. The tert-butyl carbamate handle ensures stability during synthesis, while the electron-withdrawing nitrile group enhances reactivity in downstream transformations.
(R)-2-((tert-Butoxycarbonyl)amino)-3-(3-cyanophenyl)propanoic acid serves as a valuable chiral building block in peptide and heterocyclic synthesis, enabling efficient access to bioactive scaffolds. The Boc-protected amine and pendant nitrile group offer orthogonal reactivity for selective transformations. Its bench-stable nature and compatibility with standard coupling conditions facilitate straightforward purification and integration into complex molecular architectures.
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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: