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Structure of 658-07-1
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2,6-Difluoro-4-nitrophenol delivers a potent electron-deficient aromatic scaffold featuring two fluorine substituents at the 2 and 6 positions, which enhance metabolic stability and influence regioselective reactivity. The para-nitro group serves as a strong acceptor, enabling efficient coupling in cross-coupling and nucleophilic substitution processes. This compound exhibits excellent bench stability and solubility in common organic solvents, facilitating use in synthetic workflows requiring precise electronic tuning.
2,6-Difluoro-4-nitrophenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to fluorinated heterocycles and functionalized aromatic scaffolds. Its electron-deficient aromatic ring facilitates nucleophilic aromatic substitution, while the phenolic hydroxyl group allows for direct derivatization or protection. The molecule exhibits good bench stability and compatibility with standard purification techniques, making it well-suited for multi-step synthetic sequences requiring precise regiocontrol.
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GHS Pictogram :
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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 : H302-H315-H317-H318-H410
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Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P330-P362+P364-P391-P501
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Lot numbers can be found on the outside label of a product: