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Structure of 67152-20-9
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2,4-Difluoro-5-nitrobenzonitrile features a trifunctional aromatic core with electron-withdrawing fluorine, nitro, and nitrile groups positioned for orthogonal reactivity. This bench-stable scaffold enables direct incorporation into diverse synthetic sequences, including nucleophilic substitutions and transition-metal-catalyzed couplings. The strategic placement of substituents enhances regioselective functionalization in pharmaceutical and agrochemical development.
2,4-Difluoro-5-nitrobenzonitrile serves as a versatile building block in medicinal chemistry, enabling efficient construction of functionalized heterocycles via nucleophilic aromatic substitution. Its trifunctional profile—comprising two fluorine leaving groups, a nitro group for reduction or displacement, and a nitrile for hydrolysis or coupling—facilitates modular synthesis. Bench-stable and compatible with standard reaction conditions, it supports scalable derivatization in API development 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#: 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: