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Structure of 364-78-3
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4-Fluoro-2-nitroaniline features a strategically positioned fluorine atom and nitro group on the aromatic ring, enabling selective electrophilic substitution and serving as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. This bench-stable compound integrates readily into multi-step sequences under standard conditions.
4-Fluoro-2-nitroaniline serves as a versatile building block in medicinal chemistry, enabling direct introduction of both fluorine and nitro functionalities into aromatic scaffolds. Its reactivity facilitates standard reductions to the corresponding amine, which can be further employed in Suzuki-Miyaura couplings, Ullmann reactions, or heterocycle formation. The molecule exhibits good bench stability and is compatible with common purification methods, making it well-suited for iterative synthesis workflows in API development.
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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+H312+H332-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: