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Structure of 30414-55-2
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5-Methyl-3-oxohexanoic acid methyl ester features a β-keto ester motif with a branched alkyl chain, enabling facile enolization and participation in aldol-type condensations. This structural motif supports efficient carbon–carbon bond formation under mild conditions, making it valuable for constructing complex cyclic architectures in synthetic organic chemistry.
5-Methyl-3-oxohexanoic acid methyl ester serves as a versatile β-keto ester scaffold for Claisen condensations, aldol reactions, and heterocycle synthesis. Its well-defined enolizable α-protons enable controlled carbon–carbon bond formation, while the methyl ester group supports straightforward derivatization. Bench-stable and readily purified by distillation or column chromatography, it functions reliably in multi-step synthetic sequences requiring functional group compatibility and predictable reactivity.
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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: