4-Bromo-6-chloro-1H-indazole is a heterocyclic organic compound characterized by its indazole core, which consists of a fused five-membered and six-membered ring containing nitrogen atoms. The presence of bromine and chlorine substituents at the 4 and 6 positions, respectively, contributes to its unique chemical properties and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is of interest in medicinal chemistry and pharmaceutical research due to its potential biological activity, including anti-inflammatory and anticancer properties. The presence of halogen atoms can enhance lipophilicity and influence the compound's interaction with biological targets. Additionally, 4-Bromo-6-chloro-1H-indazole can undergo various chemical reactions, such as nucleophilic substitutions and coupling reactions, making it a valuable intermediate in the synthesis of more complex molecules. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental concerns.

4-Bromo-6-chloro-1H-indazole

885519-03-9: 1H-Indazole, 4-bromo-6-chloro-, T56 Bmnj Fe Hg, 4-Bromo-6-chloro-1H-indazole

4-Bromo-6-chloro-1H-indazole is an intermediate used in the preparation of formaldoxime and hydrazine. It is prepared by diazotizing 4-chloro-2-fluoroaniline with sodium nitrite and nitrite. The product can be purified by recrystallization from water or ethanol.

CAS 885519-03-9: 4-Bromo-6-chloro-1H-indazole

4-Bromo-6-chloro-1H-indazole

Ref: IN-DA003KZ3

4-Bromo-6-chloro-1H-indazole

Ref: 10-F222393

4-Bromo-6-chloro-1H-indazole

Ref: 3D-FB140772

4-Bromo-6-chloro-1H-indazole

Ref: 54-OR951968