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Structure of 261165-06-4
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(S)-3-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid is a chiral building block featuring a para-brominated phenyl group and a protected amino functionality. This structure enables direct incorporation into peptide synthesis workflows, where the tert-butyl carbamate moiety provides stability and orthogonal deprotection compatibility. The molecule exhibits favorable solubility in common organic solvents and maintains integrity under standard bench conditions.
(S)-3-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)propanoic acid serves as a key chiral building block for synthesizing bioactive analogs, particularly in the development of peptidomimetics and heterocyclic scaffolds. The molecule combines a brominated aromatic ring with a protected α-amino acid functionality, enabling subsequent Suzuki-Miyaura coupling and selective deprotection under mild conditions. Its bench-stable tert-butyl carbamate group offers excellent functional group tolerance and simplifies purification, making it well-suited for iterative synthesis in medicinal chemistry campaigns.
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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: