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Structure of 111-79-5
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Methyl non-2-enoate is a linear, unsaturated ester featuring a conjugated double bond at the C2 position. This structure imparts enhanced reactivity in Michael additions and Diels-Alder cycloadditions. The molecule exhibits good stability under standard conditions and serves as a valuable intermediate in synthetic organic chemistry, particularly for constructing complex carbocyclic and heterocyclic frameworks.
Methyl non-2-enoate serves as a versatile synthetic building block in organic synthesis, enabling efficient access to conjugated systems via standard Michael additions, Diels-Alder reactions, and palladium-catalyzed couplings. Its α,β-unsaturated ester functionality offers predictable reactivity with nucleophiles and electrophiles, while the methyl ester group provides compatibility with standard functional group manipulations. Bench-stable and readily purified by distillation or flash chromatography, it functions effectively in multi-step syntheses of complex molecules, including natural product intermediates and pharmaceutical scaffolds.
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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: