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Structure of 325-50-8
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5-Fluoro-2-methylphenylhydrazine hydrochloride features a fluorinated aromatic ring paired with a methyl group and a hydrazine functionality, enabling selective coupling in heterocyclic synthesis. This bench-stable derivative facilitates efficient access to biologically relevant scaffolds under standard conditions.
5-Fluoro-2-methylphenylhydrazine hydrochloride serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyrazoles and other nitrogen-containing scaffolds. Its stability under standard bench conditions and compatibility with common coupling protocols facilitate straightforward incorporation into medicinal chemistry campaigns. The ortho-fluoro and methyl substituents provide predictable electronic modulation and enhanced functional group tolerance during downstream transformations.
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Lot numbers can be found on the outside label of a product: