1-Ethyl-5-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 an ethyl group at the 1-position and a nitro group at the 5-position contributes to its unique chemical properties. This compound is typically a yellow to orange solid, exhibiting moderate solubility in organic solvents. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The nitro group can participate in various chemical reactions, making it a versatile intermediate in organic synthesis. Additionally, the compound may exhibit specific reactivity patterns, such as electrophilic substitution, due to the electron-withdrawing nature of the nitro group. Safety data should be consulted, as nitro compounds can pose hazards, including toxicity and environmental concerns. Overall, 1-Ethyl-5-nitro-1H-indazole represents an interesting compound for further research in both synthetic and medicinal chemistry.

1-Ethyl-5-nitro-1H-indazole

5228-51-3: 1-Ethyl-5-nitro-1H-indazole, 1H-Indazole, 1-ethyl-5-nitro-, 1-Ethyl-5-nitroindazole

1-Ethyl-5-nitroindazole

1-Ethyl-5-nitro-1H-indazole is a six-membered ring compound that belongs to the group of nitroarenes. It has a low melting point, which makes it suitable for cleavage reactions at low temperatures. The ethyl group on the 1-position can be substituted with other groups and the nitro group can be eliminated by a substitution reaction. This leads to chains with torsion angles, which are stabilized by hydrogen bonding.

CAS 5228-51-3: 1-Ethyl-5-nitro-1H-indazole

1-Ethyl-5-nitro-1H-indazole

Ref: IN-DA00DL9G

1-Ethyl-5-nitroindazole

Ref: 54-OR910594

1-Ethyl-5-nitro-1H-indazole

Ref: 3D-FAA22851

1-Ethyl-5-nitro-1H-indazole

Ref: 10-F447855