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Structure of 170157-55-8
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This chiral building block features a (S)-configured backbone with a para-aminophenyl group and a tert-butoxycarbonyl-protected amine, enabling direct incorporation into peptide sequences. The electron-rich aromatic moiety enhances solubility in polar solvents, while the Boc group ensures stability during synthetic manipulations.
(S)-3-(3-Aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a key chiral building block for synthesizing biologically relevant heterocycles and peptidomimetics. The protected amine enables orthogonal functionalization, while the pendant aniline group facilitates coupling reactions and further derivatization. Bench-stable and readily purified by standard chromatographic methods, it functions effectively in solid-phase synthesis and solution-phase transformations.
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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: