Description Application 4-Chloroaniline can undergo: • Allylation in the presence of ultrasonication to form N-allyl-4-chloroaniline, a precursor for bioactive compounds containing indole and dihydroindole nucleus. • Povarov reaction with cyclopentadiene to form C-2 aliphatic substituted tetrahydroquinolines. • Mannich reaction with aldehydes and cyclic ketones to form β-amino carbonyl compounds. • Nitration to form 4-chloro-3-nitroaniline in the presence of guanidinium nitrate. Packaging 5, 100, 500 g in glass bottle