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Structure of 33603-63-3
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(E)-4-(Thiophen-2-yl)but-3-en-2-one features a conjugated enone system linked to a thiophene ring, enabling efficient participation in cross-coupling and cycloaddition reactions. The planar (E)-configuration enhances electronic delocalization, while the thiophene moiety provides robust stability and favorable solubility in organic solvents. This structure serves as a key building block for functionalized heterocycles and advanced materials synthesis under standard conditions.
(E)-4-(Thiophen-2-yl)but-3-en-2-one serves as a versatile synthetic building block for constructing biologically relevant heterocycles and conjugated systems. Its α,β-unsaturated ketone functionality enables reliable Michael additions, Diels-Alder reactions, and palladium-catalyzed couplings. The thiophene moiety enhances electronic delocalization and provides orthogonal reactivity, while the (E)-configuration ensures predictable stereochemical outcomes. Bench-stable and readily purified by flash chromatography, it functions efficiently in multi-step syntheses of pharmaceutical intermediates and functional materials.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: