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Structure of 32620-11-4
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(S)-2-Amino-3-methoxypropanoic acid features a chiral center with defined stereochemistry, enabling precise incorporation into peptide-based systems. The methoxy group enhances solubility and metabolic stability, while the amino and carboxylic acid functionalities support efficient coupling reactions under standard conditions. This configuration facilitates its use in bioactive molecule synthesis and structural studies.
(S)-2-Amino-3-methoxypropanoic acid serves as a valuable chiral building block for peptide mimetics and bioactive molecule synthesis. Its well-defined stereochemistry and orthogonal functional groups enable reliable incorporation into peptidomimetic scaffolds, while the methoxy group enhances solubility and metabolic stability. The compound exhibits excellent bench stability and compatibility with standard coupling protocols, facilitating efficient purification and integration into complex synthetic sequences.
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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: