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Structure of 14770-88-8
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This acrylate features a 5-methylthienyl group that imparts enhanced electron density and planarity, enabling efficient conjugation in π-stacked systems. The propenoic acid moiety provides a reactive handle for coupling reactions under mild conditions, facilitating integration into functional materials and bioconjugates.
3-(5-Methyl-2-thienyl)-2-propenoic acid serves as a versatile building block for thienyl-substituted α,β-unsaturated carboxylic acids, enabling efficient access to conjugated systems via standard Michael additions, Diels–Alder reactions, and palladium-catalyzed coupling protocols. Its bench-stable nature and tolerance to diverse functional groups facilitate straightforward incorporation into complex molecular architectures, including bioactive heterocycles and pharmaceutical scaffolds.
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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: