Halogen substituted analogoues compounds chalcone, (E)-1-(4-klorofenil)-3-p-tolilprop-2-en-1-on, was synthesized from 4-metyl benzaldehyde as aldehydes with 4-chloroacetophenone as ketones by using aldol condensation reaction. The compound resulted rendement with value of 87,51% and characterized by using UV, IR, MS, and 1HNMR. Toxicity tests using Brine Shrimp Lethality Test (BSLT) showed that those compounds have a potency as anticancer agent with LC50 value 39,8 μg/mL.
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