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Structure of 122710-21-8
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1-(2-Amino-4-methylphenyl)ethanone features a benzamide scaffold with an electron-rich aromatic ring bearing ortho-amino and para-methyl substituents. This configuration supports robust coupling reactivity in amide bond formation and enhances solubility in polar organic media. The compound serves as a key intermediate in the synthesis of bioactive heterocycles and functionalized pharmaceuticals.
1-(2-Amino-4-methylphenyl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient access to biologically relevant heterocyclic scaffolds. Its ortho-amino and methyl-substituted aromatic core facilitates palladium-catalyzed coupling reactions and cyclization processes. The compound exhibits bench stability and compatibility with standard functional group manipulations, making it well-suited for iterative synthesis campaigns in API development.
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Lot numbers can be found on the outside label of a product: