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Structure of 72185-81-0
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Methyl (S)-3-amino-2-hydroxypropanoate hydrochloride features a chiral α-amino alcohol scaffold with enhanced solubility and stability under standard conditions. This bench-stable derivative integrates seamlessly into peptide backbone modifications and serves as a key building block for bioactive molecule synthesis. The protected amine and hydroxyl groups enable selective derivatization in complex reaction sequences.
Methyl (S)-3-amino-2-hydroxypropanoate hydrochloride serves as a chiral building block for peptide mimetics and bioactive heterocycles. Its amino and hydroxyl groups enable orthogonal functionalization, while the methyl ester facilitates downstream derivatization. The hydrochloride salt enhances bench stability and solubility, supporting efficient synthesis in standard amide coupling and cyclization protocols.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: