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Structure of 917027-02-2
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This chiral building block features a protected (Boc) amine and a para-chlorophenyl group, enabling direct incorporation into peptide synthesis. The sterically hindered backbone enhances stability during coupling steps, while the electron-withdrawing chlorine improves reactivity in subsequent transformations.
(S)-2-((tert-Butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid serves as a key chiral building block for the synthesis of β-amino acid derivatives and peptidomimetics. The Boc-protected amine enables orthogonal functional group manipulation, while the para-chlorophenyl moiety provides structural rigidity and handles well under standard coupling conditions. This compound facilitates efficient peptide elongation and is compatible with diverse reaction conditions in medicinal chemistry workflows.
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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: