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Structure of 25781-92-4
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5-Chloro-2-nitro-N-phenylaniline features a chlorinated aromatic ring paired with a nitro group and an N-phenyl amine functionality, enabling its use in constructing complex heterocycles. This electron-deficient scaffold integrates readily into coupling reactions under standard conditions, offering high stability and compatibility with diverse synthetic workflows.
5-Chloro-2-nitro-N-phenylaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct access to substituted anilines via selective reduction of the nitro group. Its chlorine and nitro functionalities offer orthogonal reactivity for downstream functionalization, while the N-phenyl moiety enhances structural diversity. Bench-stable and amenable to standard purification methods, it facilitates efficient incorporation into complex heterocyclic scaffolds and API intermediates.
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Lot numbers can be found on the outside label of a product: