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Structure of 261360-77-4
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(R)-3-(3-Bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid is a chiral building block featuring a brominated aromatic ring and a protected amino group. This configuration enables direct incorporation into peptide synthesis workflows, where the tert-butyl carbamate moiety provides orthogonal stability. The para-substituted aryl handle facilitates downstream functionalization via cross-coupling reactions.
(R)-3-(3-Bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, enabling efficient access to substituted phenylalanine derivatives. The Boc-protected amine offers excellent stability and orthogonal functionality, facilitating subsequent deprotection and coupling reactions. Its brominated aryl group supports diverse cross-coupling transformations, making it ideal for constructing complex scaffolds 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: