Used as a key intermediate in the synthesis of kinase inhibitors, particularly in pharmaceutical research targeting cancer therapies. Its structure allows for selective modification, making it valuable in developing compounds that modulate protein kinase activity. Commonly employed in the preparation of potent inhibitors of JAK (Janus kinase) and other tyrosine kinases involved in inflammatory diseases and hematological malignancies. Also utilized in agrochemical research for designing bioactive molecules with pesticidal or fungicidal properties. Its bromo and chloro functional groups enable efficient cross-coupling reactions, facilitating rapid diversification in medicinal chemistry campaigns.