3-Chloro-6-methoxy-4-nitro-1H-indazole is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a chlorine atom at the 3-position, a methoxy group (-OCH3) at the 6-position, and a nitro group (-NO2) at the 4-position 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. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity in electrophilic substitution reactions. Additionally, the methoxy group can serve as a directing group in such reactions. The chlorine substituent can also affect the compound's overall polarity and potential biological activity. Overall, 3-Chloro-6-methoxy-4-nitro-1H-indazole is of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in drug development and synthesis.

3-Chloro-6-methoxy-4-nitro-1H-indazole

1000341-15-0: 1H-Indazole, 3-chloro-6-methoxy-4-nitro-, 3-Chloro-6-methoxy-4-nitro-1H-indazole

CAS 1000341-15-0: 3-Chloro-6-methoxy-4-nitro-1H-indazole

1H-Indazole, 3-chloro-6-methoxy-4-nitro-

Ref: IN-DA0000FY