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Structure of 2046-21-1
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Methyl 6-oxoheptanoate is a versatile β-keto ester featuring a ketone group at the C6 position and a methyl ester terminus. This functionalized chain enables efficient Michael additions, Claisen condensations, and cyclization reactions under mild conditions. The molecule's stability and solubility in common organic solvents support reliable performance in synthetic sequences for natural product synthesis and medicinal chemistry applications.
Methyl 6-oxoheptanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of carbocyclic and heterocyclic frameworks via aldol-type condensations and Michael additions. Its α,β-unsaturated ketone functionality facilitates regioselective transformations under mild conditions, while the ester group supports subsequent derivatization. Bench-stable and readily purified by distillation or column chromatography, it functions reliably in multi-step syntheses targeting complex natural products and pharmaceutical intermediates.
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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: