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Structure of 61275-22-7
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This chiral amide derivative features a stereodefined (S)-configuration at the α-carbon, enhancing its utility in asymmetric synthesis. The N-methyl substitution improves metabolic stability and membrane permeability, while the hydrochloride salt form ensures high solubility and ease of handling under standard conditions.
(S)-2-Amino-N-methylpropanamide hydrochloride serves as a chiral building block for peptide synthesis and bioactive molecule construction. Its well-defined stereochemistry enables stereoselective coupling reactions, while the amide and ammonium functionalities offer versatility in downstream derivatization. The hydrochloride salt enhances solubility and stability, facilitating handling and purification in standard synthetic 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: