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Structure of 275826-35-2
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(S)-3-Amino-3-(3-bromophenyl)propanoic acid features a chiral center at the alpha carbon, delivering enantioselective utility in asymmetric synthesis. The para-brominated phenyl group imparts enhanced electronic density and steric profile, facilitating downstream functionalization. This bench-stable amino acid derivative integrates readily into peptide-like scaffolds and serves as a key intermediate for bioactive molecule construction under standard conditions.
(S)-3-Amino-3-(3-bromophenyl)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and peptide-based drug discovery. Its well-defined stereochemistry and compatibility with standard amine and carboxylic acid transformations enable reliable incorporation into complex scaffolds. The bromophenyl group provides a handle for further functionalization via cross-coupling reactions, enhancing its utility in constructing diverse heterocyclic and aromatic frameworks. Bench-stable and readily purified, it functions effectively in both small-scale exploratory synthesis and process development 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: