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Structure of 3938-96-3
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Ethyl methoxyacetate was used:as acyl donor during the preparation of enantiomers of several phenylethylaminesas acylation reagent for the aminolysis of 1-phenylethanaminein an industrial, lipase-catalysed kinetic resolution of primary amine
Ethyl 2-methoxyacetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to α-alkylated esters and heterocyclic scaffolds. Its methoxy-substituted acetic acid backbone facilitates nucleophilic substitution and Claisen-type condensations under mild conditions. The compound exhibits excellent bench stability, ease of handling, and compatibility with diverse functional groups, making it ideal for iterative synthesis and scale-up applications in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Warning
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UN#: 3272
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P370+P378-P501
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Lot numbers can be found on the outside label of a product: