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Structure of 1590-25-6
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1-(6-Bromonaphthalen-2-yl)ethanone features a brominated naphthalene core paired with a ketone-functionalized ethyl side chain, enabling direct integration into cross-coupling and electrophilic substitution reactions. This bench-stable reagent delivers high regiochemical fidelity in C–C bond formation under standard conditions.
1-(6-Bromonaphthalen-2-yl)ethanone serves as a versatile building block for transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds under standard Suzuki-Miyaura and Stille conditions. The bromine substituent exhibits high reactivity and functional group tolerance, while the ketone moiety provides a handle for further derivatization via nucleophilic addition or enolization. Its bench-stable solid form facilitates handling and purification in synthetic workflows.
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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#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H319-H401
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Precautionary Statements : P264-P273-P280-P305+P351+P338-P337+P313-P501
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Lot numbers can be found on the outside label of a product: