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Structure of 10488-87-6
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Ethyl 2-methyl-3-oxo-3-phenylpropanoate features a conjugated enone system flanked by a sterically hindered methyl group and a phenyl substituent, enabling efficient Michael additions and Claisen condensations. This bench-stable ester integrates readily into complex molecular architectures under standard conditions.
Ethyl 2-methyl-3-oxo-3-phenylpropanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted benzodihydropyrans and heterocyclic scaffolds. Its α,β-unsaturated ketone functionality facilitates Michael additions and condensation reactions, while the ester group supports subsequent transformations such as hydrolysis or reduction. The molecule exhibits good bench stability and is amenable to purification via standard chromatographic methods, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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: