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Structure of 52756-36-2
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4-(tert-Butyl)-3-chloroaniline features a sterically hindered tert-butyl group flanking a chlorinated aromatic ring, delivering enhanced stability and reduced reactivity. This electron-deficient aniline derivative facilitates selective coupling reactions in synthetic pathways requiring controlled nucleophilicity.
4-(tert-Butyl)-3-chloroaniline serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering a sterically hindered arylamine with orthogonal reactivity. The tert-butyl group enhances metabolic stability and lipophilicity, while the chloro substituent enables subsequent cross-coupling reactions. Its bench-stable nature and compatibility with standard amine functionalization protocols facilitate efficient incorporation into complex molecular architectures.
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Lot numbers can be found on the outside label of a product: