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Structure of 2566-30-5
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This chiral building block features a (S)-configured stereocenter flanked by a methylamino group and a phenyl-substituted aliphatic chain, enabling selective incorporation into bioactive peptide architectures. The molecule exhibits enhanced solubility and stability under standard bench conditions, facilitating efficient coupling in solid-phase synthesis workflows.
(S)-2-(Methylamino)-3-phenylpropanoic acid serves as a key chiral building block for β-amino acid derivatives and pharmaceutically relevant scaffolds. Its well-defined stereochemistry enables reliable incorporation into peptide-like structures, while the pendant phenyl group provides structural rigidity and enhanced metabolic stability. The molecule exhibits good bench stability and facilitates straightforward purification via standard crystallization or chromatographic methods. Functions effectively in coupling reactions with minimal racemization, making it suitable for synthesis of bioactive compounds and analogs 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: