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Structure of 66762-68-3
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Ethyl 4-methoxy-3-oxobutanoate features a strategically positioned methoxy group flanking a β-keto ester moiety, enabling efficient enolization and nucleophilic addition in C–C bond formation. This scaffold integrates readily into synthetic sequences requiring controlled reactivity under mild conditions.
Ethyl 4-methoxy-3-oxobutanoate serves as a versatile synthon in carbonyl chemistry, enabling efficient access to substituted β-keto ester frameworks. Its methoxy-substituted enolizable α-carbon facilitates aldol-type condensations and Michael additions under mild conditions. The molecule exhibits bench stability and compatibility with common functional groups, simplifying purification and integration into multi-step synthetic sequences for heterocyclic and natural product synthesis.
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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: