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Structure of 261165-02-0
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This chiral building block features a (S)-configured stereocenter flanked by a brominated aromatic ring and a Boc-protected amino group. The structure enables direct incorporation into peptide backbones or conjugation workflows, offering stability under standard bench conditions and compatibility with diverse synthetic transformations.
(S)-3-(2-Bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and peptide-based drug discovery. The molecule combines a readily functionalized aryl bromide with a stable Boc-protected amino acid moiety, enabling subsequent cross-coupling reactions and orthogonal deprotection strategies. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient access to complex scaffolds.
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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: