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Structure of 7560-50-1
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Methyl-3-(4-formylphenyl)acrylate features a conjugated system linking an electron-rich aryl ring to an acrylate ester, enabling efficient Michael additions and Diels-Alder cycloadditions. The pendant aldehyde group facilitates post-functionalization via reductive amination or Wittig reactions, while the ester moiety supports selective hydrolysis. This bifunctional architecture supports rapid access to complex molecular scaffolds in synthetic organic chemistry.
Methyl-3-(4-formylphenyl)acrylate serves as a versatile synthetic building block for the construction of conjugated systems and heterocyclic scaffolds. Its dual functionality—acrylate and aldehyde—enables diverse transformations including Michael additions, Wittig reactions, and cyclizations under mild conditions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis 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 : 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: