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Structure of 84892-43-3
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4-(4-Bromophenyl)cyclohexanone features a brominated phenyl ring fused to a cyclohexanone core, delivering a robust scaffold for medicinal chemistry. This compound integrates a halogenated aromatic handle and a ketone functionality, enabling facile downstream transformations such as cross-coupling or nucleophilic addition under standard conditions.
4-(4-Bromophenyl)cyclohexanone serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biaryl-containing cyclohexanone scaffolds. Its brominated aryl group facilitates subsequent cross-coupling reactions such as Suzuki-Miyaura and Stille couplings, while the ketone functionality supports enolate formation, aldol reactions, and reductive amination. The compound exhibits good bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: