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Structure of 187242-88-2
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2-Chloro-3-nitro-6-phenylpyridine features a fused pyridine core bearing a chloro group at the 2-position, a nitro substituent at the 3-position, and a phenyl ring attached at the 6-position. This electron-deficient heterocycle serves as a key intermediate in the synthesis of functionalized pharmaceuticals and agrochemicals, offering enhanced reactivity in cross-coupling and nucleophilic substitution processes under standard conditions.
2-Chloro-3-nitro-6-phenylpyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloropyridine functionality. The ortho-nitro group enhances electrophilicity and facilitates subsequent reduction or substitution cascades. Its phenyl substituent provides steric and electronic modulation, while the molecule exhibits sufficient bench stability for routine handling. This compound functions effectively in constructing complex pharmaceutical scaffolds and functionalized aryl systems under standard reaction conditions.
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Lot numbers can be found on the outside label of a product: