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Structure of 4815-64-9
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1-Chloro-3-fluoro-5-nitrobenzene features a trifunctional aromatic core with orthogonal reactivity, enabling sequential transformations in late-stage functionalization. The electron-deficient ring supports efficient nucleophilic substitution, while the fluorine and chlorine sites offer complementary handles for cross-coupling and derivatization under mild conditions. This compound serves as a strategic intermediate in the synthesis of bioactive heterocycles and advanced pharmaceutical scaffolds.
1-Chloro-3-fluoro-5-nitrobenzene serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of complex heterocyclic systems and functionalized aromatic scaffolds. Its orthogonal reactivity profile—combining electrophilic chlorination sites with directing fluorine and nitro groups—facilitates selective metal-catalyzed coupling reactions. The molecule exhibits excellent bench stability and compatibility with standard purification techniques, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials science.
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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: