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Structure of 78881-21-7
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4-Amino-3-methylbenzonitrile features a strategically positioned amino group adjacent to a nitrile, enabling direct functionalization in pharmaceutical intermediates. The methyl substituent enhances electron density at the aromatic ring, improving reactivity in coupling processes. This bench-stable, moisture-tolerant compound integrates seamlessly into multi-step syntheses requiring controlled polarity and regioselective transformations.
4-Amino-3-methylbenzonitrile serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, quinolines, and other heterocyclic scaffolds. Its ortho-directed reactivity facilitates regioselective functionalization, while the amino and nitrile groups offer complementary handles for derivatization. The compound exhibits good bench stability and is amenable to standard purification techniques, supporting its use in multi-step synthetic sequences.
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Lot numbers can be found on the outside label of a product: