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Structure of 2596-47-6
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This acrylate derivative features a phenolic ether and ester moiety positioned ortho to the acrylic double bond, enabling conjugation with biomolecules under mild conditions. The para-acetoxy substitution enhances electrophilicity, facilitating efficient coupling reactions in bioconjugation workflows.
3-(4-Acetoxy-3-methoxyphenyl)acrylic acid serves as a versatile building block for synthesizing bioactive aromatic compounds. Its conjugated enone system enables Diels–Alder reactions and Michael additions, while the acetoxy and methoxy groups offer orthogonal protection for downstream functionalization. Bench-stable and readily purified by recrystallization, it facilitates efficient access to substituted phenylacrylates and heterocyclic scaffolds relevant to medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS07,GHS08
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Signal Word : Danger
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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-H319-H334
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Precautionary Statements : P261-P264-P270-P280-P285-P305+P351+P338-P330-P501
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Lot numbers can be found on the outside label of a product: