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Structure of 10169-55-8
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1-(4-(Phenylthio)phenyl)ethanone features a conjugated aryl-thioaryl motif with a ketone handle, enabling direct integration into cross-coupling and electrophilic functionalization sequences. This bench-stable scaffold delivers high reactivity in transition-metal-catalyzed transformations, particularly in Pd-mediated C–C bond formations.
1-(4-(Phenylthio)phenyl)ethanone serves as a versatile building block in synthetic organic chemistry, enabling the construction of biaryl and heterocyclic scaffolds. Its thioether-functionalized aryl ketone structure provides robust stability under standard reaction conditions and exhibits favorable functional group tolerance. The molecule facilitates palladium-catalyzed cross-coupling reactions and participates in electrophilic aromatic substitution processes, offering reliable access to complex molecular architectures in medicinal chemistry and materials science applications.
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H317-H318-H401-H411
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Precautionary Statements : P261-P272-P273-P280-P302+P352-P363-P391-P501
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Lot numbers can be found on the outside label of a product: