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Structure of 23943-96-6
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(R)-2-Methoxypropanoic acid is a chiral, bench-stable carboxylic acid featuring a stereodefined methoxy group at the alpha position. This configuration imparts distinct reactivity in asymmetric synthesis, enabling selective transformations in medicinal chemistry and peptide modification workflows. The molecule integrates cleanly into coupling reactions without racemization, offering reliable stereocontrol under standard conditions.
(R)-2-Methoxypropanoic acid serves as a valuable chiral building block in asymmetric synthesis, enabling stereoselective transformations through its well-defined stereochemistry and stable α-methylated carboxylic acid framework. The molecule exhibits favorable bench stability and functional group tolerance, facilitating straightforward derivatization in peptide coupling, esterification, and enantioselective catalysis. Its utility is particularly evident in the construction of bioactive scaffolds and pharmaceutical intermediates where precise stereocontrol is essential.
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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 : H319
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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: