Alectinib Intermediate

2-(4-Ethyl-3-iodophenyl)-2-methylpropanoic acid contains a phenyl ring with ethyl and iodine substituents at the para and meta positions, respectively. It also has a carboxylic acid functional group, which connects to the aromatic ring through a methylpropanoic acid linker.

2-(4-ethyl-3-iodophenyl)-2-methylpropanoic acid is predominantly used as a building block in chemical synthesis. The presence of the iodine atom allows it to undergo cross-coupling reactions (such as Suzuki or Sonogashira couplings), enabling the formation of complex biaryl structures or conjugated systems. Additionally, the carboxylic acid functionality can be converted into esters, amides, or other derivatives, which can be utilized in drug discovery processes to synthesize bioactive compounds. This compound could potentially serve as a ligand in metal-catalyzed transformations or as a core scaffold in medicinal chemistry research aimed at developing new therapeutic agents targeting specific diseases or pathways.