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Structure of 2195-47-3
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(4-Fluorophenyl)(4-nitrophenyl)methanone features a conjugated ketone bridge flanked by electron-deficient aryl groups, enabling efficient integration into cross-coupling and heterocyclic syntheses. The para-nitro group enhances reactivity in nucleophilic addition processes, while the fluorinated ring improves metabolic stability and solubility in polar organic solvents. This compound serves as a robust scaffold for pharmaceutical intermediates and functional materials.
(4-Fluorophenyl)(4-nitrophenyl)methanone serves as a versatile aryl ketone building block in synthetic organic chemistry, enabling efficient construction of biaryl and heterocyclic scaffolds. Its dual electron-withdrawing groups enhance electrophilicity at the carbonyl center, facilitating nucleophilic addition and subsequent transformations. The molecule exhibits excellent bench stability and compatibility with standard reaction conditions, simplifying purification and integration into multi-step syntheses.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: