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Structure of 316-68-7
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1-(4-Fluoronaphthalen-1-yl)ethanone features a fluorinated naphthalene core paired with a ketone handle, enabling direct integration into Suzuki-Miyaura couplings and other cross-coupling protocols. The para-fluorine enhances electrophilicity at the adjacent ring position, while the acetyl group provides a robust anchor for further functionalization under mild conditions. This compound exhibits excellent stability under standard bench handling and is compatible with diverse reaction matrices in synthetic organic chemistry workflows.
1-(4-Fluoronaphthalen-1-yl)ethanone serves as a versatile building block for constructing fluorinated naphthalene scaffolds in medicinal chemistry and materials science. Its ketone functionality enables direct nucleophilic addition, Grignard reactions, and reductive amination, while the fluoro substituent enhances metabolic stability and modulates electronic properties. The compound exhibits good bench stability and is amenable to standard purification techniques, facilitating integration into multi-step synthetic sequences.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: