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Structure of 7367-81-9
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Methyl (E)-oct-2-enoate is a conjugated ester featuring a stable (E)-configured double bond between carbons 2 and 3. This geometry imparts predictable reactivity in cross-coupling and cycloaddition processes. The methyl ester group enables direct participation in nucleophilic transformations, while the extended alkyl chain supports solubility in common organic solvents. Ideal for synthetic intermediates requiring defined stereochemistry and functional group compatibility.
Methyl (E)-oct-2-enoate serves as a versatile building block in synthetic organic chemistry, enabling stereoselective transformations via its well-defined (E)-configured double bond. Its stability under standard reaction conditions and compatibility with common functional groups facilitate efficient use in cross-coupling reactions, conjugate additions, and heterocycle synthesis. The ester moiety provides a handle for selective derivatization, making it valuable for constructing complex molecular architectures in medicinal chemistry and materials science applications.
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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 : H227-H302
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Precautionary Statements : P210-P280-P370+P378-P501
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Lot numbers can be found on the outside label of a product: