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Structure of 172921-32-3
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2,5-Difluoro-4-nitrobenzonitrile features a trifunctional aromatic core with electron-withdrawing fluorine and nitro groups flanking a nitrile moiety. This configuration imparts high reactivity in nucleophilic substitution cascades, enabling efficient access to complex heterocyclic scaffolds under mild conditions. The compound exhibits excellent bench stability and solubility in common organic solvents, facilitating use in multi-step synthetic sequences.
2,5-Difluoro-4-nitrobenzonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of fluorinated heterocycles and electron-deficient aromatic scaffolds. Its dual fluorine substituents enhance metabolic stability and modulate electronic properties, while the nitro and nitrile groups provide orthogonal reactivity for sequential transformations. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for multi-step synthetic sequences and process-scale applications.
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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: